HAYWARD, Calif., Nov. 9, 2016 /PRNewswire/ -- Impax Laboratories, Inc. (NASDAQ: IPXL), a specialty pharmaceutical company, today reported third quarter 2016 financial results for the quarter ended September 30, 2016.
Total revenues in the third quarter 2016 increased 3% to $227.9 million, compared to $221.1 million in the prior year period.
- The increase was due to a 30% increase in Specialty Pharma division revenues primarily as a result of higher sales of Rytary® and Zomig® nasal spray.
- Generic division revenues declined 3% in the third quarter 2016 compared to the prior year period as strong sales of epinephrine auto-injector (authorized generic Adrenaclick®) and oxymorphone, sales from the successful launch of three new generic products and the recent addition of products acquired from Teva Pharmaceuticals Industries Ltd. and affiliates of Allergan plc (the "Teva Transaction"), were more than offset by lower sales of diclofenac sodium gel 3% (Solaraze®), mixed amphetamine salts (Adderall XR®) and metaxalone (Skelaxin®).
On a GAAP basis, the Company recorded a per share loss of $2.51 in the third quarter 2016, compared to a gain of $0.49 per share in the prior year period. Adjusted diluted earnings per share (adjusted EPS) for the third quarter 2016 were $0.37, compared to adjusted EPS of $0.40 in the prior year period.
The third quarter 2016 GAAP results included non-cash intangible asset impairment charges of approximately $285.2 million primarily related to the Teva Transaction. The third quarter 2015 GAAP results include the impact of a gain of $45.6 million related to the sale of a Specialty Pharma product to another company. Refer to the attached "Non-GAAP Financial Measures" for a reconciliation of all GAAP to non-GAAP items.
Upon closing the Teva Transaction on August 3, 2016, the Company initiated the process of transferring and securing Teva's and Allergan's customers for the acquired products to its account. The Company assumed certain price concessions would occur following the closing, however, the Company elected to take additional price reductions on certain of the acquired products in order to retain key customers. These reductions produced significantly lower than expected operating cash flows from the acquired product lines and triggered an impairment analysis. The Company's impairment analysis resulted in the recognition of a total $251.0 million non-cash impairment charge to earnings on the Company's consolidated statement of operations for the third quarter of 2016.
"Our third quarter 2016 results reflect the volatility we have experienced as a result of additional competition on a few of our largest generic products," said Fred Wilkinson, President and Chief Executive Officer of Impax. "Successful marketing and operational strategies are helping us to capitalize on several generic opportunities, including epinephrine auto-injector and oxymorphone, and we defended our share position across the majority of our generic portfolio. That said, the ongoing impact of an increasingly challenging market environment continues to weigh on our results and consequently we are revising our outlook for fiscal 2016 to reflect the impact of lower pricing across an increased number of products in our generic portfolio."
"Despite the current industry headwinds, we remain confident that the actions we are taking will position Impax for long-term, organic growth. Within our Generics division, we intend to defend and aggressively pursue share growth of existing products, focus on maximizing new product launches, and invest in future R&D opportunities and supply chain optimization. In our Specialty division, we implemented new educational and awareness programs in an effort to accelerate Rytary and Emverm® growth. While we have implemented a number of cost saving initiatives over the past two years, given the environment, we are undertaking a review of our operating structure to ensure costs are aligned with market realities, our performance and growth assumptions. We believe the actions we are taking will enhance our ability to profitably grow in the future, while delivering value to patients and our stockholders."
Business Segment Information
The Company has two reportable segments, the Impax Generics division (generic products and services) and the Impax Specialty Pharma division (brand products and services) and does not allocate general corporate services to either segment. All information presented is on a GAAP basis unless otherwise noted.
|
Impax Generics Division Information
(Unaudited, amounts in thousands)
|
|
|
Three Months Ended
|
|
Nine Months Ended
|
|
September 30,
|
|
September 30,
|
|
2016
|
|
2015
|
|
2016
|
|
2015
|
|
Revenues:
|
|
|
|
|
|
|
|
|
Impax Generics Product sales, net
|
$ 168,593
|
|
$ 178,456
|
|
$ 455,730
|
|
$ 475,688
|
|
Rx Partner
|
6,672
|
|
1,957
|
|
11,176
|
|
6,775
|
|
Other revenues
|
55
|
|
253
|
|
188
|
|
1,623
|
|
Total revenues
|
175,320
|
|
180,666
|
|
467,094
|
|
484,086
|
|
Cost of revenues
|
115,020
|
|
112,716
|
|
307,936
|
|
299,596
|
|
Cost of revenues impairment charges
|
256,462
|
|
-
|
|
258,007
|
|
-
|
|
Gross (loss) profit
|
(196,162)
|
|
67,950
|
|
(98,849)
|
|
184,490
|
|
Operating expenses:
|
|
|
|
|
|
|
|
|
Selling, general and administrative
|
6,103
|
|
5,103
|
|
12,442
|
|
16,673
|
|
Research and development
|
15,375
|
|
14,346
|
|
46,113
|
|
38,100
|
|
In-process research and development
impairment charges
|
15,543
|
|
-
|
|
16,489
|
|
-
|
|
Patent litigation expense
|
147
|
|
397
|
|
416
|
|
2,507
|
|
Total operating expenses
|
37,168
|
|
19,846
|
|
75,460
|
|
57,280
|
|
(Loss) income from operations
|
$ (233,330)
|
|
$ 48,104
|
|
$ (174,309)
|
|
$ 127,210
|
|
|
|
|
|
|
|
|
|
Gross margin
|
(111.9%)
|
|
37.6%
|
|
(21.2%)
|
|
38.1%
|
|
Adjusted gross profit (a)
|
$ 76,873
|
|
$ 77,279
|
|
$ 192,634
|
|
$ 210,762
|
|
Adjusted gross margin (a)
|
43.8%
|
|
42.8%
|
|
41.2%
|
|
43.5%
|
|
|
(a) Adjusted gross profit is calculated as total revenues less adjusted cost of revenues. Adjusted gross margin is calculated as adjusted gross profit divided by total revenues. Refer to the "Non-GAAP Financial Measures" for a reconciliation of GAAP to non-GAAP items.
|
Total revenues for the Impax Generics division decreased 3.0% to $175.3 million in the third quarter 2016, compared to $180.7 million in the prior year period. The decrease was primarily due to the continued impact of competition on diclofenac and metaxalone, as well as lower revenue from sales of mixed amphetamine salts. These decreases were partially offset by an increase in sales and share position of epinephrine auto-injector and oxymorphone, and increased volumes from acquired products as compared to the prior year period.
Gross margin in the third quarter 2016 was a loss of 111.9% compared to gross margin of 37.6% in the prior year period. Adjusted gross margin in the third quarter 2016 increased to 43.8%, compared to adjusted gross margin of 42.8% in the prior year period. The decrease in gross margin compared to the prior year period was primarily due to an impairment charge related to the Teva Transaction, as noted above, and impairment charges related to a few products manufactured in the Company's Middlesex, New Jersey facility, which the Company is in the process of closing.
Total operating expenses in the third quarter 2016 increased $17.3 million to $37.2 million, compared to $19.8 million in the prior year period, largely due to $15.5 million of intangible asset impairment charges primarily attributable to a product acquired in the Tower Holdings, Inc. ("Tower") acquisition.
|
Impax Specialty Pharma Division Information
(Unaudited, amounts in thousands)
|
|
|
Three Months Ended
|
|
Nine Months Ended
|
|
September 30,
|
|
September 30,
|
|
2016
|
|
2015
|
|
2016
|
|
2015
|
|
Revenues:
|
|
|
|
|
|
|
|
|
Impax Specialty Pharma Product sales, net
|
$ 52,589
|
|
$ 40,206
|
|
$ 158,913
|
|
$ 93,609
|
|
Other revenues
|
-
|
|
227
|
|
-
|
|
682
|
|
Total revenues
|
52,589
|
|
40,433
|
|
158,913
|
|
94,291
|
|
Cost of revenues
|
21,853
|
|
14,834
|
|
49,916
|
|
41,147
|
|
Gross profit
|
30,736
|
|
25,599
|
|
108,997
|
|
53,144
|
|
Operating expenses:
|
3
|
|
|
|
|
|
|
|
Selling, general and administrative
|
16,358
|
|
11,418
|
|
46,309
|
|
39,186
|
|
Research and development
|
4,740
|
|
4,285
|
|
13,824
|
|
12,488
|
|
In-process research and development
impairment charges
|
13,227
|
|
-
|
|
13,227
|
|
-
|
|
Patent litigation expense
|
3,132
|
|
655
|
|
6,111
|
|
999
|
|
Total operating expenses
|
37,457
|
|
16,358
|
|
79,471
|
|
52,673
|
|
(Loss) income from operations
|
$ (6,721)
|
|
$ 9,241
|
|
$ 29,526
|
|
$ 471
|
|
|
|
|
|
|
|
|
|
Gross margin
|
58.4%
|
|
63.3%
|
|
68.6%
|
|
56.4%
|
|
Adjusted gross profit (a)
|
$ 38,152
|
|
$ 33,835
|
|
$ 127,472
|
|
$ 75,197
|
|
Adjusted gross margin (a)
|
72.5%
|
|
83.7%
|
|
80.2%
|
|
79.7%
|
|
|
(a) Adjusted gross profit is calculated as total revenues less adjusted cost of revenues. Adjusted gross margin is calculated as adjusted gross profit divided by total revenues. Refer to the "Non-GAAP Financial Measures" for a reconciliation of GAAP to non-GAAP items.
|
Total revenues for the Impax Specialty Pharma division increased 30.1% to $52.6 million in the third quarter 2016, compared to $40.4 million in the prior year period. The increase is primarily due to higher sales of Rytary and Zomig nasal spray.
Gross margin in the third quarter 2016 decreased to 58.4%, compared to 63.3% in the prior year period. Adjusted gross margin in the third quarter 2016 decreased to 72.5%, compared to adjusted gross margin of 83.7% in the prior year period. The decline in gross margin and adjusted gross margin was primarily due to higher sales of lower margin Zomig in the current year period.
Total operating expenses in the third quarter 2016 increased $21.1 million to $37.5 million, compared to $16.4 million in the prior year period, primarily due to higher research and development expense driven by impairment charges of $13.2 million relating to a product acquired in the Tower acquisition, and increased selling, general and administrative expense as a result of the sales force expansion.
|
Corporate and Other Information
(Unaudited, amounts in thousands)
|
|
|
Three Months Ended
|
|
Nine Months Ended
|
|
September 30,
|
|
September 30,
|
|
2016
|
|
2015
|
|
2016
|
|
2015
|
|
General and administrative expenses
|
$ (32,577)
|
|
$ (29,786)
|
|
$ (85,493)
|
|
$ (88,917)
|
|
Unallocated corporate expenses
|
$ (32,577)
|
|
$ (29,786)
|
|
$ (85,493)
|
|
$ (88,917)
|
|
|
|
|
|
|
|
|
|
General and administrative expenses in the third quarter 2016 increased $2.8 million to $32.6 million, compared to $29.8 million in the prior year period. The increase was principally driven by higher legal expenses and other inflationary increases, partially offset by lower business development costs.
Interest expense in the third quarter 2016 was $11.1 million, an increase of $2.9 million compared to the prior year period, which was entirely attributable to the $400 million Term Loan Facility entered into by the Company during the current year period partially to finance the Teva Transaction.
Cash and cash equivalents decreased $108.2 million to $232.1 million as of September 30, 2016, compared to $340.4 million as of December 31, 2015, primarily attributable to cash used to partially finance the Teva Transaction.
2016 Financial Guidance
The Company's full year 2016 financial guidance has been updated as of November 9, 2016, as noted below. The Company's full year 2016 estimates are based on management's current expectations, including with respect to prescription trends, pricing levels, inventory levels, and the anticipated timing of future product launches and events.
The Company does not provide forward-looking diluted earnings per share and related guidance metrics as outlined below on a GAAP basis as certain financial information, such as the amortization of recently acquired intangible assets, restructuring and impairment charges and other items used to determine such measures are not available and cannot be reasonably estimated. The following statements are forward looking and actual results could differ materially depending on market conditions and the factors set forth under "Safe Harbor" below.
- UPDATED - Total Company revenues of approximately $840 million to $855 million (previously $900 million to $940 million).
- UPDATED - Adjusted gross margins as a percent of total revenue are expected to be 48% to 50% (previously low 50% range).
- UPDATED - Adjusted research and development expenses, including patent litigation expenses, across the generic and brand divisions of approximately $90 million to $95 million (previously $100 million to $105 million).
- UPDATED - Adjusted selling, general and administrative expenses of approximately $185 million to $190 million (previously $190 million to $200 million).
- Adjusted interest expense of approximately $18 million.
- UPDATED - Capital expenditures of approximately $40 million to $50 million (previously $40 million).
- UPDATED - Adjusted EPS of approximately $1.10 to $1.20 per diluted share (previously $1.57 to $1.70).
- UPDATED - Effective tax rate of approximately 34% to 35% on a GAAP basis (previously 34% to 36%). The Company anticipates that its GAAP effective tax rate may experience volatility as the Company's tax benefits may be high compared to the Company's operating income or loss.
Conference Call Information
The Company will host a conference call with a slide presentation on November 9, 2016 at 8:30 a.m. ET to discuss its results. The call and presentation can also be accessed via a live Webcast through the Investor Relations section of the Company's Web site, www.impaxlabs.com. The number to call from within the United States is (877) 356-3814 and (706) 758-0033 internationally. The conference ID is 93578226. A replay of the conference call will be available shortly after the call for a period of seven days. To access the replay, dial (855) 859-2056 (in the U.S.) and (404) 537-3406 (international callers).
About Impax Laboratories, Inc.
Impax Laboratories, Inc. (Impax) is a specialty pharmaceutical company applying its formulation expertise and drug delivery technology to the development of controlled-release and specialty generics in addition to the development of central nervous system disorder branded products. Impax markets its generic products through its Impax Generics division and markets its branded products through the Impax Specialty Pharma division. Additionally, where strategically appropriate, Impax develops marketing partnerships to fully leverage its technology platform and pursues partnership opportunities that offer alternative dosage form technologies, such as injectables, nasal sprays, inhalers, patches, creams, and ointments. For more information, please visit the Company's Web site at: www.impaxlabs.com.
"Safe Harbor" statement under the Private Securities Litigation Reform Act of 1995:
To the extent any statements made in this news release contain information that is not historical; these statements are forward-looking in nature and express the beliefs and expectations of management. Such statements are based on current expectations and involve a number of known and unknown risks and uncertainties that could cause the Company's future results, performance, or achievements to differ significantly from the results, performance, or achievements expressed or implied by such forward-looking statements. Such risks and uncertainties include, but are not limited to: fluctuations in revenues and operating income; the Company's ability to successfully develop and commercialize pharmaceutical products in a timely manner; reductions or loss of business with any significant customer; the substantial portion of the Company's total revenues derived from sales of a limited number of products; the impact of consolidation of the Company's customer base; the impact of competition; the Company's ability to sustain profitability and positive cash flows; any delays or unanticipated expenses in connection with the operation of the Company's manufacturing facilities; the effect of foreign economic, political, legal, and other risks on the Company's operations abroad; the uncertainty of patent litigation and other legal proceedings; the increased government scrutiny on the Company's agreements with brand pharmaceutical companies; product development risks and the difficulty of predicting FDA filings and approvals; consumer acceptance and demand for new pharmaceutical products; the impact of market perceptions of the Company and the safety and quality of the Company's products; the Company's determinations to discontinue the manufacture and distribution of certain products; the Company's ability to achieve returns on its investments in research and development activities; changes to FDA approval requirements; the Company's ability to successfully conduct clinical trials; the Company's reliance on third parties to conduct clinical trials and testing; the Company's lack of a license partner for commercialization of NUMIENTTM (IPX066) outside of the United States; impact of illegal distribution and sale by third parties of counterfeits or stolen products; the availability of raw materials and impact of interruptions in the Company's supply chain; the Company's policies regarding returns, allowances and chargebacks; the use of controlled substances in the Company's products; the effect of current economic conditions on the Company's industry, business, results of operations and financial condition; disruptions or failures in the Company's information technology systems and network infrastructure caused by third party breaches or other events; the Company's reliance on alliance and collaboration agreements; the Company's reliance on licenses to proprietary technologies; the Company's dependence on certain employees; the Company's ability to comply with legal and regulatory requirements governing the healthcare industry; the regulatory environment; the effect of certain provisions in the Company's government contracts; the Company's ability to protect its intellectual property; exposure to product liability claims; risks relating to goodwill and intangibles; changes in tax regulations; the Company's ability to manage growth, including through potential acquisitions and investments; the risks related to the Company's acquisitions of or investments in technologies, products or businesses; the restrictions imposed by the Company's credit facility and indenture; the Company's level of indebtedness and liabilities and the potential impact on cash flow available for operations; uncertainties involved in the preparation of the Company's financial statements; the Company's ability to maintain an effective system of internal control over financial reporting; the effect of terrorist attacks on the Company's business; the location of the Company's manufacturing and research and development facilities near earthquake fault lines; expansion of social media platforms and other risks described in the Company's periodic reports filed with the Securities and Exchange Commission. Forward-looking statements speak only as to the date on which they are made, and the Company undertakes no obligation to update publicly or revise any forward-looking statement, regardless of whether new information becomes available, future developments occur or otherwise.
Company Contact:
Mark Donohue
Investor Relations and Corporate Communications
(215) 558-4526
www.impaxlabs.com
|
Impax Laboratories, Inc.
Consolidated Statements of Operations
(Unaudited, amounts in thousands, except share and per share data)
|
|
|
Three Months Ended
|
|
Nine Months Ended
|
|
September 30,
|
|
September 30,
|
|
2016
|
|
2015
|
|
2016
|
|
2015
|
|
Revenues:
|
|
|
|
|
|
|
|
|
Impax Generics, net
|
$ 175,320
|
|
$ 180,666
|
|
$ 467,094
|
|
$ 484,086
|
|
Impax Specialty Pharma, net
|
52,589
|
|
40,433
|
|
158,913
|
|
94,291
|
|
Total revenues
|
227,909
|
|
221,099
|
|
626,007
|
|
578,377
|
|
Cost of revenues
|
136,873
|
|
127,550
|
|
357,852
|
|
340,743
|
|
Cost of revenues impairment charges
|
256,462
|
|
-
|
|
258,007
|
|
-
|
|
Gross (loss) profit
|
(165,426)
|
|
93,549
|
|
10,148
|
|
237,634
|
|
Operating expenses:
|
|
|
|
|
|
|
|
|
Selling, general and administrative
|
55,038
|
|
46,307
|
|
144,244
|
|
144,776
|
|
Research and development
|
20,115
|
|
18,631
|
|
59,937
|
|
50,588
|
|
In-process research and development
impairment charges
|
28,770
|
|
-
|
|
29,716
|
|
-
|
|
Patent litigation expense
|
3,279
|
|
1,052
|
|
6,527
|
|
3,506
|
|
Total operating expenses
|
107,202
|
|
65,990
|
|
240,424
|
|
198,870
|
|
(Loss) income from operations
|
(272,628)
|
|
27,559
|
|
(230,276)
|
|
38,764
|
|
Other expense, net:
|
|
|
|
|
|
|
|
|
Interest expense
|
(11,089)
|
|
(8,182)
|
|
(27,874)
|
|
(19,110)
|
|
Interest income
|
222
|
|
247
|
|
895
|
|
825
|
|
Reserve for Turing receivable
|
-
|
|
-
|
|
(48,043)
|
|
-
|
|
Loss on debt extinguishment
|
-
|
|
-
|
|
-
|
|
(16,903)
|
|
Gain on sale of asset
|
-
|
|
45,574
|
|
-
|
|
45,574
|
|
Net change in fair value of derivatives
|
-
|
|
(4,000)
|
|
-
|
|
(4,000)
|
|
Other, net
|
(373)
|
|
134
|
|
(14)
|
|
929
|
|
(Loss) income before income taxes
|
(283,868)
|
|
61,332
|
|
(305,312)
|
|
46,079
|
|
(Benefit from) provision for income taxes
|
(104,531)
|
|
25,577
|
|
(112,866)
|
|
18,509
|
|
Net (loss) income
|
$ (179,337)
|
|
$ 35,755
|
|
$ (192,446)
|
|
$ 27,570
|
|
|
|
|
|
|
|
|
|
Net (loss) income per share:
|
|
|
|
|
|
|
|
|
Basic
|
$ (2.51)
|
|
$ 0.51
|
|
$ (2.71)
|
|
$ 0.40
|
|
Diluted
|
$ (2.51)
|
|
$ 0.49
|
|
$ (2.71)
|
|
$ 0.38
|
|
|
|
|
|
|
|
|
|
Weighted-average common shares outstanding:
|
|
|
|
|
|
|
|
Basic
|
71,331,247
|
|
69,820,348
|
|
71,033,346
|
|
69,378,792
|
|
Diluted
|
71,331,247
|
|
72,777,746
|
|
71,033,346
|
|
72,548,557
|
|
Impax Laboratories, Inc.
Condensed Consolidated Balance Sheets
(Unaudited, amounts in thousands)
|
|
|
September 30,
|
|
December 31,
|
|
2016
|
|
2015
|
|
Assets
|
|
|
|
|
Current assets:
|
|
|
|
|
Cash and cash equivalents
|
$ 232,123
|
|
$ 340,351
|
|
Accounts receivable, net
|
239,590
|
|
324,451
|
|
Inventory, net
|
167,554
|
|
125,582
|
|
Prepaid expenses and other assets
|
61,319
|
|
31,689
|
|
Total current assets
|
700,586
|
|
822,073
|
|
Property, plant and equipment, net
|
227,588
|
|
214,156
|
|
Intangible assets, net
|
891,225
|
|
602,020
|
|
Goodwill
|
208,382
|
|
210,166
|
|
Deferred income taxes
|
36,666
|
|
315
|
|
Other non-current assets
|
55,209
|
|
73,757
|
|
Total assets
|
$ 2,119,656
|
|
$ 1,922,487
|
|
|
|
|
|
Liabilities and Stockholders' Equity
|
|
|
|
|
Current liabilities:
|
|
|
|
|
Accounts payable and accrued expenses
|
$ 297,066
|
|
$ 261,036
|
|
Accrued profit sharing and royalty expenses
|
19,759
|
|
65,725
|
|
Current portion of long-term debt
|
17,708
|
|
-
|
|
Total current liabilities
|
334,533
|
|
326,761
|
|
Long-term debt, net
|
812,375
|
|
424,595
|
|
Deferred income taxes
|
-
|
|
72,770
|
|
Other non-current liabilities
|
68,888
|
|
35,952
|
|
Total liabilities
|
1,215,796
|
|
860,078
|
|
Total stockholders' equity
|
903,860
|
|
1,062,409
|
|
Total liabilities and stockholders' equity
|
$ 2,119,656
|
|
$ 1,922,487
|
|
Impax Laboratories, Inc.
Condensed Consolidated Statements of Cash Flows
(Unaudited, amounts in thousands)
|
|
|
|
Nine Months Ended
|
|
|
September 30,
|
|
|
2016
|
|
2015
|
|
Cash flows from operating activities:
|
|
|
|
|
Net (loss) income
|
$ (192,446)
|
|
$ 27,570
|
|
Adjustments to reconcile net (loss) income to net cash provided by operating activities:
|
|
|
|
|
Depreciation and amortization
|
63,101
|
|
48,664
|
|
Non-cash interest expense
|
16,604
|
|
6,026
|
|
Share-based compensation expense
|
23,375
|
|
21,851
|
|
Tax impact related to the exercise of employee stock options and vesting of restricted
stock awards
|
(507)
|
|
(5,213)
|
|
Deferred income taxes - net and uncertain tax positions
|
(94,703)
|
|
(8,833)
|
|
Intangible asset impairment charges
|
287,723
|
|
-
|
|
Accrued profit sharing and royalty expense, net of payments
|
(45,966)
|
|
16,004
|
|
Reserve for Turing receivable
|
48,043
|
|
-
|
|
Gain on sale of asset
|
-
|
|
(45,574)
|
|
Loss on debt extinguishment
|
-
|
|
16,903
|
|
Net change in fair value of derivatives
|
-
|
|
4,000
|
|
Provision for inventory reserves
|
14,779
|
|
(10,204)
|
|
Other
|
23
|
|
(762)
|
|
Changes in assets and liabilities which provided (used) cash
|
(22,258)
|
|
(35,356)
|
|
Net cash provided by operating activities
|
97,768
|
|
35,076
|
|
|
|
|
|
|
Cash flows from investing activities:
|
|
|
|
|
Payment for acquisition, net of cash acquired
|
(585,800)
|
|
(691,348)
|
|
Proceeds from sale of intangible assets
|
-
|
|
59,546
|
|
Purchases of property, plant and equipment
|
(31,860)
|
|
(14,709)
|
|
Proceeds from sale of property, plant and equipment
|
1,346
|
|
-
|
|
Payments for licensing agreements
|
(3,500)
|
|
(5,550)
|
|
Proceeds from repayment of Tolmar loan
|
15,000
|
|
-
|
|
Maturities of short-term investments
|
-
|
|
200,064
|
|
Net cash used in investing activities
|
(604,814)
|
|
(451,997)
|
|
|
|
|
|
|
Cash flows from financing activities:
|
|
|
|
|
Proceeds from sale of convertible notes
|
-
|
|
600,000
|
|
Proceeds from issuance of term loan
|
400,000
|
|
435,000
|
|
Repayment of term loan
|
-
|
|
(435,000)
|
|
Payment of deferred financing fees
|
(11,867)
|
|
(36,941)
|
|
Purchase of bond hedge derivative asset
|
-
|
|
(147,000)
|
|
Proceeds from sale of warrants
|
-
|
|
88,320
|
|
Tax impact related to the exercise of employee stock options and vesting of restricted
stock awards
|
507
|
|
5,213
|
|
Proceeds from exercise of stock options and ESPP
|
9,137
|
|
10,928
|
|
Net cash provided by financing activities
|
397,777
|
|
520,520
|
|
|
|
|
|
|
Effect of exchange rate changes on cash and cash equivalents
|
1,041
|
|
(70)
|
|
Net (decrease) increase in cash and cash equivalents
|
(108,228)
|
|
103,529
|
|
Cash and cash equivalents, beginning of period
|
340,351
|
|
214,873
|
|
Cash and cash equivalents, end of period
|
$ 232,123
|
|
$ 318,402
|
|
Impax Laboratories, Inc.
Non-GAAP Financial Measures
|
|
|
Adjusted net income, adjusted net income per diluted share, EBITDA, adjusted EBITDA, adjusted cost of revenues, adjusted research and development expenses and adjusted selling, general and administrative expenses are not measures of financial performance under generally accepted accounting principles (GAAP) and should not be construed as substitutes for, or superior to, GAAP net (loss) income, GAAP net (loss) income per diluted share, GAAP cost of revenues, GAAP research and development expenses and GAAP selling, general and administrative expenses as a measure of financial performance. However, management uses both GAAP financial measures and the disclosed non-GAAP financial measures internally to evaluate and manage the Company's operations and to better understand its business. Further, management believes the addition of non-GAAP financial measures provides meaningful supplementary information to, and facilitates analysis by, investors in evaluating the Company's financial performance, results of operations and trends. The Company's calculations of adjusted net income, adjusted net income per diluted share, EBITDA, adjusted EBITDA, adjusted cost of revenues, adjusted research and development expenses and adjusted selling, general and administrative expenses, may not be comparable to similarly designated measures reported by other companies, since companies and investors may differ as to what type of events warrant adjustment.
|
|
|
The following table reconciles reported net (loss) income to adjusted net income.
(Unaudited, amounts in thousands, except per share data)
|
|
|
Three months ended
|
|
Nine Months Ended
|
|
September 30,
|
|
September 30,
|
|
2016
|
|
2015
|
|
2016
|
|
2015
|
|
Net (loss) income
|
$ (179,337)
|
|
$ 35,755
|
|
$ (192,446)
|
|
$ 27,570
|
|
Adjusted to add (deduct):
|
|
|
|
|
|
|
|
|
Amortization (a)
|
18,367
|
|
10,307
|
|
39,604
|
|
27,216
|
|
Business development expenses (b)
|
2,072
|
|
3,682
|
|
4,289
|
|
14,971
|
|
Hayward facility remediation costs (c)
|
-
|
|
3,546
|
|
-
|
|
9,391
|
|
Tower acquisition severance (d)
|
-
|
|
-
|
|
-
|
|
2,411
|
|
Philadelphia packaging and distribution restructuring (e)
|
84
|
|
2,767
|
|
88
|
|
5,410
|
|
Middlesex manufacturing restructuring (f)
|
5,516
|
|
-
|
|
12,103
|
|
-
|
|
Payments for licensing agreements (g)
|
622
|
|
750
|
|
922
|
|
750
|
|
Fair value of inventory step-up (h)
|
-
|
|
1,104
|
|
-
|
|
6,467
|
|
Ticking Fees (i)
|
-
|
|
-
|
|
-
|
|
2,317
|
|
Non-cash interest expense (j)
|
5,890
|
|
5,097
|
|
16,605
|
|
5,097
|
|
Reserve for Turing receivable (k)
|
-
|
|
-
|
|
48,043
|
|
-
|
|
Intangible asset impairment charges (l)
|
285,232
|
|
-
|
|
287,723
|
|
-
|
|
Loss on debt extinguishment (m)
|
-
|
|
-
|
|
-
|
|
16,903
|
|
Gain on sale of asset (n)
|
-
|
|
(45,574)
|
|
-
|
|
(45,574)
|
|
Net change in fair value of derivatives (o)
|
-
|
|
4,000
|
|
-
|
|
4,000
|
|
Deferred financing costs (p)
|
-
|
|
-
|
|
-
|
|
928
|
|
Turing legal expenses (q)
|
5,443
|
|
-
|
|
5,443
|
|
-
|
|
Lease termination for office consolidation (r)
|
144
|
|
-
|
|
144
|
|
-
|
|
Income tax effect (s)
|
(117,884)
|
|
7,772
|
|
(150,504)
|
|
(17,858)
|
|
Adjusted net income
|
$ 26,149
|
|
$ 29,206
|
|
$ 72,014
|
|
$ 59,999
|
|
|
|
|
|
|
|
|
|
Adjusted net income per diluted share
|
$ 0.37
|
|
$ 0.40
|
|
$ 1.00
|
|
$ 0.83
|
|
Net (loss) income per diluted share
|
$ (2.51)
|
|
$ 0.49
|
|
$ (2.71)
|
|
$ 0.38
|
|
Diluted weighted-average common shares outstanding
|
71,542
|
|
72,778
|
|
71,840
|
|
72,549
|
|
Impax Laboratories, Inc.
Non-GAAP Financial Measures
|
|
|
(a)
|
Reflects amortization of intangible assets which increased substantially during the third quarter 2016 compared to the prior year period, due to the current period acquisition of a portfolio of generic products from Teva and affiliates of Allergan plc (the "Teva Transaction"). Amortization expense also includes the March 2015 acquisition of Tower (including its operating subsidiaries CorePharma LLC and Amedra Pharmaceuticals LLC) and Lineage Therapeutics Inc. Included in "Cost of revenues" on the Consolidated Statements of Operations.
|
|
(b)
|
Professional fees related to business development activities related to the third quarter 2016 Teva Transaction. Prior year amounts are related to the Tower acquisition and integration-related activities. Included in "Selling, general and administrative" expenses on the Consolidated Statements of Operations.
|
|
(c)
|
Remediation costs related to the Hayward, California manufacturing facility. Included in "Cost of revenues" on the Consolidated Statements of Operations.
|
|
(d)
|
Related to the Tower acquisition. Included in "Selling, general and administrative" expense on the Consolidated Statements of Operations.
|
|
(e)
|
Costs related to the closing of the Company's packaging and distribution facilities in Pennsylvania. Included in "Cost of revenues" and "Other expense, net" on the Consolidated Statements of Operations.
|
|
(f)
|
In March 2016, the Company announced the closure of its Middlesex, New Jersey manufacturing and packaging site and a related reduction in workforce at the site over the following 24 months. Included in "Cost of revenues" on the Consolidated Statements of Operations.
|
|
(g)
|
During the third quarter 2016, the Company made a milestone payment to a third party partner under the terms of a Research and Development Agreement. Included in "Research and development" expense on the Consolidated Statements of Operations.
|
|
(h)
|
Fair value adjustment of inventory as a result of purchase accounting for the Tower acquisition. Included in "Cost of revenues" on the Consolidated Statements of Operations.
|
|
(i)
|
Fees incurred relating to the Company's $435.0 million term loan with Barclays Bank PLC to lock in the financing terms beginning from the lenders' commitment of the term loan to the actual allocation of the term loan upon the closing of the Tower transaction. The term loan was subsequently terminated by the Company on June 30, 2015. Included in "Interest expense" on the Consolidated Statements of Operations.
|
|
(j)
|
Related to non-cash accretion of debt discount attributable to deferred financing costs associated with the $400 million term loan to finance the Teva Transaction, the $435.0 million term loan and $600.0 million of outstanding 2% convertible senior notes and bifurcation of the conversion option of the convertible notes. Included in "Interest expense" on the Consolidated Statements of Operations.
|
|
(k)
|
The Company recorded a reserve in the amount of $48.0 million representing the full amount of the estimated receivable due from Turing Pharmaceuticals AG as of March 31, 2016, as a result of the uncertainty of the Company collecting the reimbursement amounts owed by Turing. The $48.0 million reserve was unchanged as of September 30, 2016. Included as a separate line item on the Consolidated Statements of Operations.
|
|
(l)
|
During the third quarter of 2016, the Company recognized a total of $285.2 million of intangible asset impairment charges, of which $251.0 million related to the Teva Transaction. The impairment charge related to the Teva Transaction comprised of a $248.0 million charge recorded in "Cost of revenues impairment charges" and a $3.0 million charge to "In-process research and development impairment charges" expense on the Consolidated Statements of Operations. During the third quarter of 2016, the Company also recognized $25.7 million of intangible asset impairment charges related to two of the Company's in-process research and development (IPR&D) product rights acquired from Tower due to delays in expected start of commercialization and lower pricing amid highly competitive market conditions, resulting in lower expected future cash flows, included in "In-process research and development impairment charges" expense, and $8.5 million attributable to the full impairment of three marketed products and one third-party partnered product where the Company received royalties, included in "Cost of revenues impairment charges" on the Consolidated Statements of Operations.
|
|
(m)
|
Loss on the extinguishment and repayment of the $435.0 million term loan with Barclays Bank PLC due to the write-off of $16.9 million of deferred financing costs. Included in "Loss on debt extinguishment" on the Consolidated Statements of Operations.
|
|
(n)
|
In July 2015, the Company received an unsolicited offer from Turing Pharmaceuticals AG to purchase the U.S. rights to Daraprim®, one of the intangible assets acquired in the Tower acquisition, as well as the active pharmaceutical ingredient for the product and the finished goods inventory on hand. The sale closed in August 2015, pursuant to which the Company received proceeds of $55.5 million at closing. The carrying value of the Daraprim rights at the time of the closing was $9.3 million. The Company recognized a gain on sale of intangible asset of $45.6 million, net of expenses. Included as a separate line item on the Consolidated Statements of Operations. As the inventory was sold at cost, there was no gain or loss recognized.
|
|
(o)
|
The Company recognized $4.0 million of expense related to the net change in the fair value of its derivative instruments from June 30, 2015 to September 30, 2015. Included in "Net change in fair value of derivatives" on the Consolidated Statements of Operations.
|
|
(p)
|
Amortization of financing costs related to the Company's $435.0 million term loan with Barclays Bank PLC. Included in "Interest expense" on the Consolidated Statements of Operations.
|
|
(q)
|
Legal fees incurred as a result of the Company's litigation against Turing alleging breach of the terms of the Turing Asset Purchase Agreement for failure to reimburse the Company for chargebacks and Medicaid rebate liability. Included in "Selling, general and administrative" expenses on the Consolidated Statements of Operations.
|
|
(r)
|
During the third quarter 2016, the Company consolidated its three Pennsylvania locations into a new leased facility in Fort Washington, Pennsylvania. Included in "Cost of revenues" and "Selling, general and administrative" expenses on the Consolidated Statements of Operations.
|
|
(s)
|
Adjusted income taxes are calculated by tax effecting adjusted pre-tax income at the applicable effective tax rate that will be determined by reference to statutory tax rates in the relevant jurisdiction in which the Company operates and includes current and deferred income tax expense commensurate with the non-GAAP measure of profitability.
|
|
Impax Laboratories, Inc.
Non-GAAP Financial Measures
(Unaudited, amounts in thousands)
|
|
|
The following table reconciles reported net (loss) income to adjusted EBITDA.
|
|
|
Three months ended
|
|
Nine Months Ended
|
|
September 30,
|
|
September 30,
|
|
2016
|
|
2015
|
|
2016
|
|
2015
|
|
Net (loss) income
|
$ (179,337)
|
|
$ 35,755
|
|
$ (192,446)
|
|
$ 27,570
|
|
Adjusted to add (deduct):
|
|
|
|
|
|
|
|
|
Interest income
|
(222)
|
|
(247)
|
|
(895)
|
|
(825)
|
|
Interest expense
|
11,089
|
|
8,182
|
|
27,874
|
|
19,110
|
|
Depreciation and amortization
|
25,059
|
|
17,949
|
|
59,350
|
|
48,664
|
|
Income taxes
|
(104,531)
|
|
25,577
|
|
(112,866)
|
|
18,509
|
|
EBITDA
|
(247,942)
|
|
87,216
|
|
(218,983)
|
|
113,028
|
|
|
|
|
|
|
|
|
|
Adjusted to add (deduct):
|
|
|
|
|
|
|
|
|
Business development expenses
|
2,072
|
|
3,682
|
|
4,289
|
|
14,971
|
|
Hayward facility remediation costs
|
-
|
|
3,546
|
|
-
|
|
9,391
|
|
Tower acquisition severance
|
-
|
|
-
|
|
-
|
|
2,411
|
|
Philadelphia packaging and distribution restructuring
|
84
|
|
2,767
|
|
88
|
|
5,410
|
|
Middlesex manufacturing restructuring
|
5,516
|
|
-
|
|
12,103
|
|
-
|
|
Payments for licensing agreements
|
622
|
|
750
|
|
922
|
|
750
|
|
Fair value of inventory step-up
|
-
|
|
1,104
|
|
-
|
|
6,467
|
|
Reserve for Turing receivable
|
-
|
|
-
|
|
48,043
|
|
-
|
|
Intangible asset impairment charges
|
285,232
|
|
-
|
|
287,723
|
|
-
|
|
Loss on debt extinguishment
|
-
|
|
-
|
|
-
|
|
16,903
|
|
Net change in fair value of derivatives
|
-
|
|
4,000
|
|
-
|
|
4,000
|
|
Gain on sale of asset
|
-
|
|
(45,574)
|
|
-
|
|
(45,574)
|
|
Turing legal expenses
|
5,443
|
|
-
|
|
5,443
|
|
-
|
|
Lease termination for office consolidation
|
144
|
|
-
|
|
144
|
|
-
|
|
Share-based compensation
|
7,713
|
|
8,292
|
|
23,375
|
|
21,851
|
|
Adjusted EBITDA
|
$ 58,884
|
|
$ 65,783
|
|
$ 163,147
|
|
$ 149,608
|
|
Impax Laboratories, Inc.
Non-GAAP Financial Measures
(Unaudited, amounts in thousands)
|
|
|
The following table reconciles reported cost of revenues, research and development expenses, and selling, general and administrative expenses to adjusted cost of revenues, adjusted gross profit, adjusted gross margin, adjusted research and development expenses, and adjusted selling, general and administrative expenses.
|
|
|
Three months ended
|
|
Nine Months Ended
|
|
September 30,
|
|
September 30,
|
|
2016
|
|
2015
|
|
2016
|
|
2015
|
|
Cost of revenues
|
$ 136,873
|
|
$ 127,550
|
|
$ 357,852
|
|
$ 340,743
|
|
Adjusted to deduct:
|
|
|
|
|
|
|
|
|
Amortization
|
18,367
|
|
10,307
|
|
39,604
|
|
27,216
|
|
Hayward facility remediation costs
|
-
|
|
3,546
|
|
-
|
|
9,391
|
|
Philadelphia packaging and distribution restructuring
|
53
|
|
2,608
|
|
191
|
|
5,251
|
|
Middlesex manufacturing restructuring
|
5,516
|
|
-
|
|
12,103
|
|
-
|
|
Lease termination for office consolidation
|
53
|
|
-
|
|
53
|
|
-
|
|
Fair value of inventory step-up
|
-
|
|
1,104
|
|
-
|
|
6,467
|
|
Adjusted cost of revenues
|
$ 112,884
|
|
$ 109,985
|
|
$ 305,901
|
|
$ 292,418
|
|
|
|
|
|
|
|
|
|
Adjusted gross profit (a)
|
$ 115,025
|
|
$ 111,114
|
|
$ 320,106
|
|
$ 285,959
|
|
Adjusted gross margin (a)
|
50.5%
|
|
50.3%
|
|
51.1%
|
|
49.4%
|
|
|
|
|
|
|
|
|
|
Research and development expenses
|
$ 20,115
|
|
$ 18,631
|
|
$ 59,937
|
|
$ 50,588
|
|
Adjusted to deduct:
|
|
|
|
|
|
|
|
|
Payments for licensing agreements
|
622
|
|
750
|
|
922
|
|
750
|
|
Adjusted research and development expenses
|
$ 19,493
|
|
$ 17,881
|
|
$ 59,015
|
|
$ 49,838
|
|
|
|
|
|
|
|
|
|
Selling, general and administrative expenses
|
$ 55,038
|
|
$ 46,307
|
|
$ 144,244
|
|
$ 144,776
|
|
Adjusted to deduct:
|
|
|
|
|
|
|
|
|
Business development expenses
|
2,072
|
|
3,682
|
|
4,289
|
|
14,971
|
|
Tower acquisition severance
|
-
|
|
-
|
|
-
|
|
2,411
|
|
Philadelphia packaging and distribution restructuring
|
31
|
|
159
|
|
72
|
|
159
|
|
Turing legal expenses
|
5,443
|
|
-
|
|
5,443
|
|
-
|
|
Lease termination for office consolidation
|
91
|
|
-
|
|
91
|
|
-
|
|
Adjusted selling, general and administrative expenses
|
$ 47,401
|
|
$ 42,466
|
|
$ 134,349
|
|
$ 127,235
|
|
|
(a) Adjusted gross profit is calculated as total revenues less adjusted cost of revenues. Adjusted gross margin is calculated as adjusted gross profit divided by total revenues.
|
|
Impax Laboratories, Inc.
Non-GAAP Financial Measures
(Unaudited, amounts in thousands)
|
|
|
The following tables reconcile the Impax Generics and Impax Specialty Pharma Divisions reported cost of revenues to adjusted cost of revenues, adjusted gross profit and adjusted gross margin.
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Impax Generics Division Information
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Three months ended
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Nine Months Ended
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September 30,
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September 30,
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2016
|
|
2015
|
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2016
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2015
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Cost of revenues
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$ 115,020
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$ 112,716
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$ 307,936
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$ 299,596
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Adjusted to deduct:
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|
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|
|
|
|
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Amortization
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10,951
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|
3,083
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|
21,129
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|
10,538
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Hayward facility remediation costs
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-
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|
3,546
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|
-
|
|
9,391
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Philadelphia packaging and distribution restructuring
|
53
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|
2,608
|
|
191
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|
5,251
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Middlesex manufacturing restructuring
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5,516
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|
-
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|
12,103
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|
-
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Lease termination for office consolidation
|
53
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|
-
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|
53
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|
-
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Fair value of inventory step-up
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-
|
|
92
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|
-
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|
1,092
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Adjusted cost of revenues
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$ 98,447
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$ 103,387
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$ 274,460
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|
$ 273,324
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|
|
|
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Adjusted gross profit (a)
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$ 76,873
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|
$ 77,279
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|
$ 192,634
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$ 210,762
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Adjusted gross margin (a)
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43.8%
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|
42.8%
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|
41.2%
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43.5%
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Impax Specialty Pharma Division Information
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|
|
Three months ended
|
|
Nine Months Ended
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|
September 30,
|
|
September 30,
|
|
2016
|
|
2015
|
|
2016
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|
2015
|
|
Cost of revenues
|
$ 21,853
|
|
$ 14,834
|
|
$ 49,916
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|
$ 41,147
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Adjusted to deduct:
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|
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|
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Amortization
|
7,416
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|
7,224
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|
18,475
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|
16,678
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Fair value of inventory step-up
|
-
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1,012
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|
-
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|
5,375
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Adjusted cost of revenues
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$ 14,437
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$ 6,598
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$ 31,441
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$ 19,094
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|
|
|
|
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Adjusted gross profit (a)
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$ 38,152
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$ 33,835
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$ 127,472
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$ 75,197
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Adjusted gross margin (a)
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72.5%
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83.7%
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80.2%
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|
79.7%
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(a) Adjusted gross profit is calculated as total revenues less adjusted cost of revenues. Adjusted gross margin is calculated as adjusted gross profit divided by total revenues.
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To view the original version on PR Newswire, visit:http://www.prnewswire.com/news-releases/impax-reports-third-quarter-2016-financial-results-300359706.html
SOURCE Impax Laboratories, Inc.