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AMAG Pharmaceuticals Reports Third Quarter 2016 Financial Results and Provides Corporate Update

Total GAAP quarterly revenue increased 50% to $143.8 million, driven by record sales of Makena®

Significant growth in operating and net income

Next-generation development programs progressing well

Conference call scheduled for 8:00 a.m. ET today

WALTHAM, Mass., Nov. 03, 2016 (GLOBE NEWSWIRE) -- AMAG Pharmaceuticals, Inc. (NASDAQ:AMAG) today reported unaudited consolidated financial results for the third quarter ended September 30, 2016. Total revenue for the third quarter of 2016 increased approximately 50% to $143.8 million. This increase was driven by record sales of Makena and the recognition of a full quarter of revenue from Cord Blood Registry® (CBR), which was acquired by AMAG on August 17, 2015. The company reported third quarter 2016 operating income of $38.8 million and net income of $16.2 million. Non-GAAP adjusted EBITDA for the third quarter of 2016 increased to $76.2 million1, or 44%, versus the same period in 2015. Non-GAAP net income for the third quarter of 2016 increased to $61.8 million1, or 46%, versus the same period in 2015.

"We executed well against our key priorities in the third quarter, delivering strong financial results and hitting key milestones in our next-generation development programs," stated William Heiden, AMAG's chief executive officer. "Our Makena subcutaneous auto-injector program is on-track for an sNDA filing in the second quarter of next year and the Feraheme sNDA submission seeking approval of a broader label has been accelerated to mid-year 2017."

"We have updated the company's financial guidance based on our fourth quarter expectations of continued strong top and bottom line performance, building on our successes achieved in the third quarter,” Mr. Heiden continued.

Third Quarter 2016 and Recent Business Highlights

  • Delivered total revenue of $143.8 million in the third quarter of 2016, compared with $96.2 million in the same period last year. This increase of approximately 50% was driven by record sales of Makena and the recognition of a full quarter of revenue from CBR.
  • Achieved Makena sales of $93.4 million in the third quarter of 2016, compared with $65.2 million in the same period last year. Makena's robust sales growth of 43% was driven exclusively by an increase in volume. This growth resulted in Makena market share of 41%, four percentage points over the second quarter of 2016 and an 11 percentage point gain year-to-date.
  • Generated 1.8% growth to $29.9 million1 in non-GAAP revenue from CBR over the second quarter of 2016 due to improved net revenue per new customer. In addition, enrollments were higher versus the second quarter of 2016.
  • Reported $22.3 million in Feraheme sales, maintaining market share in the intravenous iron market, which experienced a slight decline in the third quarter of 2016.
  • Achieved key milestones in the Makena subcutaneous auto-injector development program. The company dosed first subjects in both the definitive pharmacokinetic study and comparative pain study. Data from each of these studies is intended to support the supplemental new drug application (sNDA) that the company plans to file with the Food and Drug Administration (FDA) in the second quarter of 2017.
  • Continued to enroll patients more rapidly than expected in the company’s head-to-head, Phase 3 clinical trial evaluating Feraheme in adults with iron deficiency anemia (IDA). The company is seeking to broaden Feraheme’s current label beyond its chronic kidney disease (CKD) indication to include all adult IDA patients who have failed or cannot tolerate oral iron treatment. The timeline to anticipated approval has been shortened by approximately six months as a result of the trial’s rapid enrollment, which has accelerated the company's expected sNDA submission date to mid-2017.
  • Generated an increase of $147.8 million in cash and investments in the first nine months of 2016 to $614.1 million, net of $20.0 million utilized to repurchase the company’s common stock and $13.1 million to repay debt.

Third Quarter Ended September 30, 2016 (unaudited)

Financial Results (GAAP Basis)
Total revenues for the third quarter of 2016 were $143.8 million, compared with $96.2 million in the third quarter of 2015. This increase is related to record sales of Makena and the recognition of a full quarter of revenue from CBR, which was acquired by AMAG on August 17, 2015. Net product sales of Makena increased to $93.4 million in the third quarter of 2016, compared with $65.2 million in the same period last year. This 43% growth in Makena sales was primarily driven by the successful launch of the single-dose, preservative-free formulation and strong growth in the company’s Makena @Home program. Sales of Feraheme and MuGard® totaled $22.4 million in the third quarter of 2016, compared with $23.8 million in the third quarter of 2015. Service revenue from CBR totaled $28.0 million in the third quarter of 2016, as compared to $7.2 million in the third quarter of 2015.

Total costs and expenses, including costs of product sales and services, totaled $105.0 million for the third quarter of 2016, compared with $97.5 million for the same period in 2015. The increase in operating expenses in 2016 was related to: (i) higher research and development expenses for the company's next generation development programs, (ii) higher selling, general and administrative expenses due to the recognition of a full quarter of CBR-related expenses, and (iii) higher non-cash amortization of the Makena intangible asset. These increases were partially offset by expenses in the third quarter of 2015 that did not recur in 2016 related to an upfront payment for AMAG's exclusive option to acquire rights to a development stage asset to treat severe preeclampsia (Velo) and CBR-related acquisition costs.

Third quarter 2016 operating income totaled $38.8 million, compared with a $1.4 million loss in the third quarter of last year. The company reported net income of $16.2 million, or $0.47 per basic share and $0.43 per diluted share, for the third quarter of 2016, compared with a net loss of $20.6 million, or $0.62 per basic and diluted share, for the same period in 2015.

Balance Sheet Highlights
The company’s cash, cash equivalents and investments increased by $147.8 million in the first nine months of 2016 to approximately $614.1 million, net of $20.0 million utilized to repurchase the company’s common stock and $13.1 million to repay debt. Total debt (principal amount outstanding), including $200 million of convertible debt, was approximately $1.03 billion as of September 30, 2016. For the 12 months ended September 30, 2016, sales of Makena exceeded $300 million, triggering a $100 million milestone that will be paid to former Lumara Health shareholders in the fourth quarter of 2016.

"In the third quarter, we once again generated strong cash flow as a result of our solid commercial execution and operating discipline,” stated Ted Myles, chief financial officer of AMAG. "We are now in an even better position to capitalize on acquisition or licensing opportunities that would diversify and expand our product portfolio."

Financial Results (Non-GAAP Basis)1,2
Non-GAAP revenues totaled $145.8 million in the third quarter of 2016, up from $103.5 million in the third quarter of 2015. Non-GAAP CBR revenue totaled $29.9 million in the third quarter of 2016, compared with $14.5 million in the same period in 2015. CBR's financial results for the third quarter of 2015 include only a portion of the quarter, as AMAG purchased CBR on August 17, 2015. The difference between GAAP and non-GAAP revenue for the quarter represents purchase accounting adjustments related to CBR deferred revenue.

Total non-GAAP costs and expenses, including costs of product sales and services, totaled $69.6 million in the third quarter of 2016, compared with total non-GAAP costs and expenses of $50.6 million in the same period in 2015. Non-GAAP adjusted EBITDA for the third quarter of 2016 was $76.2 million, compared with $52.8 million for the same period in 2015.

The company generated third quarter 2016 non-GAAP net income of $61.8 million, or $1.81 per non-GAAP basic share and $1.78 per non-GAAP diluted share. In the third quarter of 2015, non-GAAP net income totaled $42.3 million, or $1.27 per non-GAAP basic share and $1.02 per non-GAAP diluted share. Non-GAAP diluted shares for the third quarter of 2016 do not include 7.4 million of potentially dilutive shares from the convertible notes, as the stock price was below the convertible notes' exercise price.

Updated 2016 Financial Guidance Range3

2016 GAAP Guidance 2016 Non-GAAP Guidance
$ in millions PreviousUpdated PreviousUpdated
Makena sales $310 - $340$330 - $340 $310 - $340$330 - $340
Feraheme and MuGard sales $95 - $105$95 - $105 $95 - $105$95 - $105
CBR revenue $98 - $108$98 - $108 $115 - $125$115 - $125
Total revenue $503 - $553$523 - $553 $520 - $570$540 - $570
Net income $0 - $30$3 - $23 $195 - $225$200 - $220
Operating income $93 - $123$98 - $118 N/AN/A
Adjusted EBITDA N/AN/A $255 - $285$260 - $280

Conference Call and Webcast Access
AMAG Pharmaceuticals, Inc. will host a conference call and webcast with slides today at 8:00 a.m. ET, during which management will discuss the company’s financial and operating results and recent developments. To access the conference call via telephone, please dial (877) 412-6083 from the United States or (702) 495-1202 for international access. A telephone replay will be available from approximately 11:00 a.m. ET on November 3, 2016 through midnight on November 10, 2016. To access a replay of the conference call, dial (855) 859-2056 from the United States or (404) 537-3406 for international access. The pass code for the live call and the replay is 96588865.

The call will be webcast with slides and accessible through the Investors section of the company’s website at www.amagpharma.com. The webcast replay will be available from approximately 11:00 a.m. ET on November 3, 2016 through midnight on December 3, 2016.

Use of Non-GAAP Financial Measures
AMAG has presented certain non-GAAP financial measures, including non-GAAP revenues, non-GAAP costs and expenses, non-GAAP adjusted EBITDA (earnings before income taxes, depreciation and amortization), non-GAAP net income and non-GAAP basic and diluted net income per share. These non-GAAP financial measures exclude certain amounts, revenue, expenses, income or dilutive shares from the corresponding financial measures determined in accordance with accounting principles generally accepted in the U.S. (GAAP).

Management believes this non-GAAP information is useful for investors, taken in conjunction with AMAG’s GAAP financial statements, because it provides greater transparency regarding AMAG’s operating performance and prospects for future performance and allows investors to better compare performance over different periods. Management uses these measures, among other factors, to assess and analyze operational results and trends and to make financial and operational decisions, including in compensation decisions. Non-GAAP information is not prepared under a comprehensive set of accounting rules and should only be used to supplement an understanding of AMAG’s operating results as reported under GAAP, not as a substitute for GAAP financial measures, and AMAG encourages investors to review its consolidated financial statements and publicly filed reports in their entirety. In addition, these non-GAAP financial measures are unlikely to be comparable with non-GAAP information provided by other companies. Due to the adjustments made to GAAP net income (loss) and GAAP net income (loss) per share to calculate non-GAAP net income and non-GAAP net income per share, the non-GAAP measures are higher than GAAP net income (loss) and GAAP net income (loss) per share. Non-GAAP net income and non-GAAP net income per share should not be considered measures of our liquidity. The determination of the amounts that are excluded from non-GAAP financial measures is a matter of management judgment and depends upon, among other factors, the nature of the underlying expense or income amounts. Reconciliations between these non-GAAP financial measures and the most comparable GAAP financial measures are included in the tables accompanying this press release after the unaudited condensed consolidated financial statements.

About AMAG
AMAG is a biopharmaceutical company focused on developing and delivering important therapeutics, conducting clinical research in areas of unmet need and creating education and support programs for the patients and families we serve. Our products support the health of patients in the areas of maternal health, anemia management and cancer supportive care. Through CBR®, we also help families to preserve newborn stem cells, which are used today in transplant medicine for certain cancers and blood, immune and metabolic disorders, and have the potential to play a valuable role in the ongoing development of regenerative medicine. For additional company information, please visit www.amagpharma.com.

About Makena® (hydroxyprogesterone caproate injection)
Makena® is a progestin indicated to reduce the risk of preterm birth in women pregnant with a single baby who have a history of singleton spontaneous preterm birth.

The effectiveness of Makena is based on improvement in the proportion of women who delivered <37 weeks of gestation. There are no controlled trials demonstrating a direct clinical benefit, such as improvement in neonatal mortality and morbidity.

Limitation of use: While there are many risk factors for preterm birth, safety and efficacy of Makena has been demonstrated only in women with a prior spontaneous singleton preterm birth. It is not intended for use in women with multiple gestations or other risk factors for preterm birth.

Makena should not be used in women with any of the following conditions: blood clots or other blood clotting problems, breast cancer or other hormone-sensitive cancers, or history of these conditions; unusual vaginal bleeding not related to the current pregnancy, yellowing of the skin due to liver problems during pregnancy, liver problems, including liver tumors, or uncontrolled high blood pressure. Before patients receive Makena, they should tell their healthcare provider if they have an allergy to hydroxyprogesterone caproate, castor oil, or any of the other ingredients in Makena; diabetes or prediabetes, epilepsy, migraine headaches, asthma, heart problems, kidney problems, depression, or high blood pressure.

In one clinical study, certain complications or events associated with pregnancy occurred more often in women who received Makena. These included miscarriage (pregnancy loss before 20 weeks of pregnancy), stillbirth (fetal death occurring during or after the 20th week of pregnancy), hospital admission for preterm labor, preeclampsia (high blood pressure and too much protein in the urine), gestational hypertension (high blood pressure caused by pregnancy), gestational diabetes, and oligohydramnios (low amniotic fluid levels).

Makena may cause serious side effects including blood clots, allergic reactions, depression, and yellowing of the skin and the whites of the eyes. The most common side effects of Makena include injection site reactions (pain, swelling, itching, bruising, or a hard bump), hives, itching, nausea, and diarrhea.

For additional product information, including full prescribing information, please visit www.makena.com.

About Feraheme® (ferumoxytol)
Feraheme received marketing approval from the FDA on June 30, 2009 for the treatment of IDA in adult CKD patients and was commercially launched by AMAG in the U.S. shortly thereafter. Ferumoxytol is protected in the U.S. by six issued patents covering the composition and dosage form of the product. Each issued patent is listed in the FDA’s Orange Book, the last of which expires in June 2023.

Fatal and serious hypersensitivity reactions including anaphylaxis have occurred in patients receiving Feraheme. Initial symptoms may include hypotension, syncope, unresponsiveness, cardiac/cardiorespiratory arrest. Feraheme is contraindicated in patients with a known hypersensitivity to Feraheme or any of its components, or a history of allergic reaction to any intravenous iron product.

For additional product information, please see full Prescribing Information, including Boxed Warning, available at www.feraheme.com.

About Cord Blood Registry® (CBR)
CBR is the world’s largest private newborn stem cell company. Founded in 1992, CBR is entrusted by parents with storing more than 600,000 umbilical cord blood and cord tissue units. CBR is dedicated to advancing the clinical application of newborn stem cells by partnering with reputable research institutions on FDA-regulated clinical trials for conditions that have no cure today. For more information, visit www.cordblood.com.

Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 (PSLRA) and other federal securities laws. Any statements contained herein which do not describe historical facts, including, among others, expectations for AMAG’s next generation development programs for Makena, including the anticipated timing to file an sNDA; expectations for AMAG’s Phase 3 clinical trial for the broader indication for Feraheme, including the anticipated timing of an sNDA submission; AMAG’s 2016 updated financial guidance, including GAAP and non-GAAP revenues, GAAP operating income, non-GAAP adjusted EBITDA and GAAP and non-GAAP net income; AMAG's intention to pay a $100 million milestone to former Lumara Health shareholders in the fourth quarter of 2016; AMAG’s belief that the generation of strong cash flows in the first nine months of 2016 puts AMAG in a better position to diversify and expand its portfolio; and beliefs that newborn stem cells have the potential to play a valuable role in the development of regenerative medicine are forward-looking statements which involve risks and uncertainties that could cause actual results to differ materially from those discussed in such forward-looking statements.

Such risks and uncertainties include, among others, those risks identified in AMAG’s filings with the U.S. Securities and Exchange Commission (SEC), including its Annual Report on Form 10-K for the year ended December 31, 2015, its Quarterly Reports on Form 10-Q for the quarters ended March 31, 2016 and June 30, 2016 and subsequent filings with the SEC. Any such risks and uncertainties could materially and adversely affect AMAG’s results of operations, its profitability and its cash flows, which would, in turn, have a significant and adverse impact on AMAG’s stock price. AMAG cautions you not to place undue reliance on any forward-looking statements, which speak only as of the date they are made.

AMAG disclaims any obligation to publicly update or revise any such statements to reflect any change in expectations or in events, conditions or circumstances on which any such statements may be based, or that may affect the likelihood that actual results will differ from those set forth in the forward-looking statements.

AMAG Pharmaceuticals® and Feraheme® are registered trademark of AMAG Pharmaceuticals, Inc. MuGard® is a registered trademark of Abeona Therapeutics, Inc. Makena® is a registered trademark of AMAG Pharmaceuticals IP, Ltd. Cord Blood Registry® and CBR® are registered trademarks of CBR Systems, Inc.

1
See summaries of GAAP to non-GAAP adjustments at the conclusion of this press release.
2See share count reconciliation at the conclusion of this press release.
3See reconciliation of 2016 financial guidance of non-GAAP adjusted EBITDA and non-GAAP net income at the conclusion of this press release.

- Tables Follow -

AMAG Pharmaceuticals, Inc.
Condensed Consolidated Statements of Operations
(unaudited, amounts in thousands, except for per share data)
Three Months Ended September 30, Nine Months Ended September 30,
2016 2015 2016 2015
Revenues:
Makena $93,387 $65,155 $236,824 $184,258
Feraheme/MuGard 22,390 23,762 71,500 66,726
Cord Blood Registry 27,965 7,177 71,863 7,177
License fee, collaboration and other revenues 40 58 313 51,380
Total revenues 143,782 96,152 380,500 309,541
Operating costs and expenses:
Cost of product sales 25,706 19,088 65,942 59,793
Cost of services 4,984 3,261 15,705 3,261
Research and development expenses 17,116 9,809 45,579 24,981
Option rights to license orphan drug 10,000 10,000
Selling, general and administrative expenses 57,216 46,141 172,314 110,054
Impairment charges of intangible assets 15,963
Acquisition-related costs 8,500 11,153
Restructuring expenses 738 712 1,752
Total costs and expenses 105,022 97,537 316,215 220,994
Operating income 38,760 (1,385) 64,285 88,547
Other income (expense):
Interest expense (18,309) (14,222) (55,002) (34,794)
Loss on debt extinguishment (10,449) (10,449)
Interest and dividend income 838 524 2,319 967
Other income (expense) (24) (9,182) 197 (9,180)
Total other income (expense) (17,495) (33,329) (52,486) (53,456)
Income (loss) before income taxes 21,265 (34,714) 11,799 35,091
Income tax expense (benefit) 5,069 (14,130) 3,725 9,513
Net income (loss) $16,196 $(20,584) $8,074 $25,578
Net income (loss) per share
Basic $0.47 $(0.62) $0.23 $0.84
Diluted $0.43 $(0.62) $0.23 $0.73
Weighted average shares outstanding used to compute net income (loss) per share:
Basic 34,171 33,223 34,377 30,379
Diluted 42,111 33,223 34,764 34,962


AMAG Pharmaceuticals, Inc.
Condensed Consolidated Balance Sheets
(unaudited, amounts in thousands)
September 30, 2016 December 31, 2015
ASSETS
Current assets:
Cash and cash equivalents$305,279 $228,705
Investments308,792 237,626
Accounts receivable, net70,079 85,678
Inventories38,157 40,645
Receivable from collaboration 428
Prepaid and other current assets14,474 13,592
Total current assets736,781 606,674
Property, plant and equipment, net25,255 28,725
Goodwill639,484 639,188
Intangible assets, net1,122,535 1,196,771
Restricted cash2,593 2,593
Other long-term assets1,005 2,259
Total assets$2,527,653 $2,476,210
LIABILITIES AND STOCKHOLDERS’ EQUITY
Current liabilities:
Accounts payable$4,742 $4,906
Accrued expenses126,363 106,363
Current portion of long-term debt62,791 17,500
Current portion of acquisition-related contingent consideration100,359 96,967
Deferred revenues34,653 20,185
Total current liabilities328,908 245,921
Long-term liabilities:
Long-term debt, net747,869 803,669
Convertible 2.5% notes, net177,146 170,749
Acquisition-related contingent consideration127,094 125,592
Deferred tax liabilities192,608 189,145
Deferred revenues12,513 5,093
Other long-term liabilities3,562 3,777
Total liabilities1,589,700 1,543,946
Total stockholders’ equity937,953 932,264
Total liabilities and stockholders’ equity$2,527,653 $2,476,210


AMAG Pharmaceuticals, Inc.
Reconciliation of Non-GAAP Adjustments to Net Income
(unaudited, amounts in thousands)
Three Months Ended September 30, Nine Months Ended September 30,
2016 2015 2016 2015
GAAP revenues$143,782 $96,152 $380,500 $309,541
Service revenues1,985 47,321 415,600 47,321 4
License fee, collaboration and other revenues (39,965)5
Non-GAAP revenues145,767 103,473 396,100 276,897
GAAP CBR revenues27,965 7,177 71,863 7,177
Service revenues1,985 47,321 415,600 47,321 4
Non-GAAP CBR revenues29,950 14,498 87,463 14,498
GAAP costs of product sales and services30,690 22,349 81,647 63,054
Cost of product sales(20,915)6(15,336)6(53,151)6(49,597)6
Cost of services(359)7(215)7(1,072)7(215)7
Non-GAAP costs of product sales and services9,416 6,798 27,424 13,242
GAAP costs and expenses105,022 97,537 316,215 220,994
Cost of product sales(20,915)6(15,336)6(53,151)6(49,597)6
Cost of services(359)7(215)7(1,072)7(215)7
Research and development expenses(901)8(1,550)8(3,541)8(3,241)8
Selling, general and administrative expenses(13,244)9(10,561)9(33,971)9(20,246)9
Option rights to license orphan drug (10,000)10 (10,000)10
Impairment charges of intangible assets (15,963)11
Acquisition-related costs (8,500)12 (11,153)12
Restructuring expenses (738)13(712)13(1,752)13
Non-GAAP costs and expenses69,603 50,637 207,805 124,790
GAAP other income (expense), including income tax expense (benefit)(22,564) (19,199) (56,211) (62,969)
Non-cash interest expense3,171 143,111 149,333 148,943 14
Loss on debt extinguishment 10,449 15 10,449 15
Other income (expense) 9,187 16 9,185 16
Income tax expense (benefit)5,069 17(14,130)173,725 179,513 17
Non-GAAP other income (expense)(14,324) (10,582) (43,153) (24,879)
GAAP net income (loss)16,196 (20,584) 8,074 25,578
Total adjustments45,644 62,838 137,068 101,650
Non-GAAP net income (loss)61,840 42,254 145,142 127,228


4Represents purchase accounting adjustments related to deferred revenue in connection with the CBR acquisition.
5Represents adjustments to exclude certain non-cash revenue associated with the 2014 termination of the company’s ex-US ferumoxytol marketing agreement.
6Adjustments to eliminate the following: (i) non-cash step-up of inventory from purchase accounting; (ii) amortization expense related to intangible assets; (iii) depreciation expense; and (iv) stock-based compensation expense.
7Adjustments to eliminate depreciation expense.
8Adjustments to eliminate the following: (i) non-cash step-up of inventory used in research and development from purchase accounting; (ii) depreciation expense; and (iii) stock-based compensation expense.
9Adjustments to eliminate the following: (i) non-cash adjustments related to contingent consideration; (ii) amortization expense related to intangible assets; (iii) depreciation expense; and (iv) stock-based compensation expense.
10Eliminate one-time costs related to Velo option.
11Impairment expense of $15.7 million related to the MuGard intangible asset and $0.2 million related to the favorable lease intangible asset
12Adjustments to eliminate one-time costs related to CBR acquisition.
13Adjustments to eliminate non-recurring restructuring costs.
14Adjustments to eliminate non-cash interest expense.
15Eliminate non-cash or one-time expenses related to the August 2015 term loan refinancing.
16Eliminate one-time expenses related to the August 2015 debt financing.
17Adjustments to eliminate non-cash income tax expense (benefit).


AMAG Pharmaceuticals, Inc.
Reconciliation of GAAP Net Income (Loss) to Non-GAAP Net Income to Non-GAAP Adjusted EPS
(unaudited, amounts in thousands, except per share data)
Three Months Ended September 30, Nine Months Ended September 30,
2016 2015 2016 2015
GAAP Net Income (Loss)$16,196 $(20,584) $8,074 $25,578
Adjustments:
Interest expense, net17,471 13,698 52,683 33,827
Loss on debt extinguishment 10,449 10,449
Other income24 9,182 (197) 9,180
Provision for income tax5,069 (14,130) 3,725 9,513
Operating income38,760 (1,385) 64,285 88,547
Purchase accounting adjustments related to CBR deferred revenue1,985 7,321 15,600 7,321
Non-cash collaboration revenue (39,965)
Depreciation and intangible asset amortization24,672 15,350 65,104 40,333
Non-cash inventory step-up adjustments1,573 2,122 4,718 11,948
Stock-based compensation5,468 4,889 16,808 11,572
Adjustments to contingent consideration3,708 2,886 5,106 4,525
Option rights to license orphan drug 10,000 10,000
Impairment charges of intangible assets 15,963
Acquisition-related costs 10,901 13,735
Restructuring costs 753 712 4,090
Non-GAAP adjusted EBITDA76,166 52,837 188,296 152,106
Cash interest(14,323) (10,582) (43,154) (24,879)
Non-GAAP Net Income$61,843 $42,255 $145,142 $127,227
Basic:
GAAP net income (loss) per share - Basic$0.47 $(0.62) $0.23 $0.84
Shares used in GAAP per share computation34,171 33,223 34,377 30,379
Non-GAAP net income per share - Basic$1.81 $1.27 $4.22 $4.19
Shares used in non-GAAP per share computation 34,171 33,223 34,377 30,379
Diluted:
GAAP net income (loss) per share - Diluted$0.43 $(0.62) $0.23 $0.73
Shares used in GAAP per share computation42,111 33,223 34,764 34,962
Non-GAAP net income per share - Diluted$1.78 $1.02 $4.18 $3.31
Shares used in non-GAAP per share computation 34,730 41,229 34,764 38,430


AMAG Pharmaceuticals, Inc.
Reconciliation of 2016 Financial Guidance of Non-GAAP Adjusted EBITDA and Non-GAAP Net Income
(unaudited, amounts in millions)
2016 Financial Guidance
Previous Updated
GAAP Net Income$0 - $30 $3 - $23
Adjustments:
Interest expense73 73
Provision for income tax20 22
Operating income$93 - $123 $98 - $118
Purchase accounting adjustments related to CBR deferred revenue17 17
Depreciation and intangible asset amortization91 91
Non-cash inventory step-up adjustments5 5
Stock-based compensation26 26
Adjustments to contingent consideration6 6
Impairment charges of intangible assets16 16
Restructuring costs1 1
Non-GAAP adjusted EBITDA$255 - $285 $260 - $280
Cash interest(60) (60)
Non-GAAP Net Income$195 - $225 $200 - $220


AMAG Pharmaceuticals, Inc.
Share Count Reconciliation
(unaudited, amounts in millions)
Three Months Ended September 30, Nine Months Ended September 30,
2016 2015 2016 2015
Weighted average basic shares outstanding 34.2 33.2 34.4 30.4
Employee equity incentive awards 0.5 18 0.4 1.6
Convertible notes 7.4 18 18 18
Warrants 18 18 18 3.0
GAAP diluted shares outstanding 42.1 33.2 34.8 35.0
Employee equity incentive awards 1.5 19
Convertible notes (7.4)19 7.4 19 7.4 19
Effect of bond hedge and warrants (0.9)20 (4.0)20
Non-GAAP diluted shares outstanding 34.7 41.2 34.8 38.4


18Employee equity incentive awards, convertible notes and warrants would be anti-dilutive in this period utilizing the “if-converted” method, which adjusts net income for the after-tax interest expense applicable to the convertible notes.
19Reflects the Non-GAAP dilutive impact of employee equity incentive awards and convertible notes.
20Reflects the impact of the non-GAAP benefit of the bond hedge and warrants.

CONTACT: AMAG Pharmaceuticals, Inc. Linda Lennox Vice President, Investor Relations 617-498-2846

Source:AMAG Pharmaceuticals, Inc.