DOCSLIB.ORG

31AUG201819403718 Before Casting Your Vote

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
31AUG201819403718 Before Casting Your Vote 31AUG201819403718 April 20, 2020 ASSERTIO LETTER TO STOCKHOLDERS MERGER PROPOSED—YOUR VOTE IS VERY IMPORTANT Assertio Therapeutics, Inc. (‘‘Assertio Therapeutics’’ or ‘‘Assertio’’) entered into an Agreement and Plan of Merger dated as of March 16, 2020, which is referred to in this Joint Proxy Statement/Prospectus as the ‘‘Merger Agreement,’’ with Zyla Life Sciences (‘‘Zyla’’) and certain wholly-owned subsidiaries of Assertio formed to effectuate the Merger Agreement. Pursuant to the Merger Agreement and through a series of transactions described in this Joint Proxy Statement/Prospectus and referred to as the ‘‘Merger,’’ Zyla and Assertio will become wholly-owned subsidiaries of Assertio Holdings, Inc. (‘‘Assertio Holdings’’), with Assertio Holdings assuming Assertio’s listing on the Nasdaq Stock Market. The Merger Agreement is attached as Annex A to this Joint Proxy Statement/Prospectus and is incorporated into this Joint Proxy Statement/Prospectus by reference. This Joint Proxy Statement/Prospectus describes the Merger Agreement, the Merger and the transactions related to the Merger in detail and provides information concerning the annual meeting of Assertio stockholders (the ‘‘Assertio Annual Meeting’’). At the effective time of the Merger (the ‘‘Effective Time’’), each issued and outstanding share of common stock, $0.001 par value per share, of Zyla (‘‘Zyla Common Stock’’) will be converted into the right to receive 2.5 shares of common stock, $0.0001 par value per share, of Assertio Holdings (‘‘Assertio Holdings Common Stock’’). The exact amount of stock consideration to be received in the Merger in exchange for shares of Zyla Common Stock cannot be determined until the Effective Time. See ‘‘The Agreement and Plan of Merger—Consideration in the Merger’’ in Chapter I of this Joint Proxy Statement/Prospectus on page 161. Assertio’s board of directors has unanimously approved the Merger Agreement, the Merger and the issuance of shares of Assertio Holdings Common Stock in the Merger. The issuance of shares of Assertio Holdings Common Stock in the Merger requires the approval of a majority of the outstanding shares of common stock, $0.0001 par value per share, of Assertio (‘‘Assertio Common Stock’’) present at the Assertio Annual Meeting and entitled to vote on the matter (Assertio Proposal 1 in this Joint Proxy Statement/ Prospectus). Assertio stockholders will vote at the Assertio Annual Meeting on May 19, 2020, at 1:00 p.m., Central Time. In light of ongoing developments related to coronavirus (COVID-19), after careful consideration, Assertio’s board of directors has determined that the Assertio Annual Meeting will be a virtual meeting conducted exclusively via live webcast in order to facilitate stockholder attendance and participation while safeguarding the health of Assertio stockholders, Assertio’s board of directors and the Assertio management team. Assertio stockholders or their proxyholder will be able to attqend the Assertio Annual Meeting online, vote and submit questions by visiting https://www.cstproxy.com/assertiotx/2020 and using a control number assigned by Continental Stock Transfer. To register and receive access to the virtual meeting, registered stockholders and beneficial stockholders (those holding shares through a stock brokerage account or by a bank or other holder of record) will need to follow the instructions applicable to them provided in the enclosed Joint Proxy Statement/Prospectus. Before casting your vote, please take the time to review carefully this Joint Proxy Statement/Prospectus, including the section entitled ‘‘Risk q Factors’’ in Chapter I of this Joint Proxy Statement/Prospectus beginning on page 34. Your vote is very important regardless of the number of shares you hold. Our board of directors recommends that you vote ‘‘FOR’’ the approval of the issuance of shares of Assertio Holdings Common Stock in the Merger. Arthur J. Higgins President and Chief Executive Officer Assertio Therapeutics, Inc. Neither the Securities and Exchange Commission nor any state securities regulator has approved or disapproved the securities to be issued under this Joint Proxy Statement/Prospectus or determined if this Joint Proxy Statement/Prospectus is accurate or adequate. Any representation to the contrary is a criminal offense. This Joint Proxy Statement/Prospectus is dated April 20, 2020 and is first being mailed to Assertio stockholders and Zyla stockholders on or about April 20, 2020. 31AUG201819403718 ASSERTIO THERAPEUTICS, INC. 100 SOUTH SAUNDERS ROAD, SUITE 300 LAKE FOREST, ILLINOIS 60045 NOTICE OF ANNUAL MEETING OF STOCKHOLDERS Online Meeting Only—https://www.cstproxy.com/assertiotx/2020 To Be Held on May 19, 2020 1:00 p.m. Central Time To the stockholders of Assertio Therapeutics, Inc.: Notice is hereby given that the Annual Meeting of Stockholders of Assertio Therapeutics, Inc., a Delaware corporation (‘‘Assertio’’), will be held at on May 19, 2020 at 1:00 p.m., Central Time (the ‘‘Assertio Annual Meeting’’). In light of ongoing developments related to coronavirus (COVID-19), and the related protocols that federal, state and local governments have implemented, Assertio’s board of directors has determined that the Assertio Annual Meeting will be a virtual meeting conducted exclusively via live webcast. Assertio’s board of directors believes that this is the right choice for Assertio and Assertio’s stockholders at this time, as it permits stockholders to attend and participate in the Assertio Annual Meeting while safeguarding the health of Assertio stockholders, Assertio’s board of directors and the Assertio management team. We are committed to ensuring that Assertio stockholders will be afforded the same rights and opportunities to participate as they would at an in-person meeting. You can attend the meeting by visiting https://www.cstproxy.com/assertiotx/2020 where you will be able to listen to the meeting live, submit questions and vote online. To participate in the virtual meeting, you will need the 16-digit control number assigned by Continental Stock Transfer included on your proxy card or voting instruction form. To register and receive access to the virtual meeting, registered stockholders and beneficial stockholders (those holding shares through a stock brokerage account or by a bank or other holder of record) will need to follow the instructions applicable to them provided in the enclosed Joint Proxy Statement/Prospectus. The meeting webcast will begin promptly at 1:00 p.m., Central Time. We encourage you to access the meeting prior to the start time. Online check-in will begin at 12:30 p.m., Central Time, and you should allow ample time for the check-in procedures. If you experience technical difficulties during the check-in process or during the Assertio Annual Meeting please call (917) 262-2373 for assistance. For additional information on how you can attend and participate in the virtual Assertio Annual Meeting, please see the instructions beginning on page 206 of the attached Joint Proxy Statement/Prospectus. Because the Assertio Annual Meeting will be a completely virtual meeting, there will be no physical location for stockholders to attend. Assertio is holding the meeting for the following purposes, as more fully described in the accompanying Joint Proxy Statement/Prospectus: 1. To approve the issuance of shares of common stock, $0.0001 par value per share, of Assertio Holdings, Inc. (‘‘Assertio Holdings Common Stock’’) in connection with the Merger with Zyla Life Sciences, as described in greater detail in Chapter I of this Joint Proxy Statement/ Prospectus. 2. To elect the nine directors of Assertio named in the attached Joint Proxy Statement/ Prospectus to serve until the 2021 Annual Meeting of Stockholders, or until their successors are duly elected and qualified. 3. To approve an increase in the number of shares available for issuance under Assertio’s Amended and Restated 2014 Omnibus Incentive Plan, a copy of which is attached as Annex G to this Joint Proxy Statement/Prospectus. If the proposal to issue stock in connection with the Merger (Proposal 1) is not approved, the proposal to increase the number of shares available under Assertio’s Amended and Restated 2014 Omnibus Incentive Plan will be automatically withdrawn. 4. To approve an increase in the number of shares available for issuance under Assertio’s Amended and Restated 2004 Employee Stock Purchase Plan, a copy of which is attached as Annex H to this Joint Proxy Statement/Prospectus. 5. To approve an amendment to Assertio’s certificate of incorporation to effect a reverse stock split at a ratio of not less than 1-for-2 and not greater than 1-for-4. 6. To approve, on an advisory basis, the compensation of Assertio’s named executive officers. 7. To approve, on an advisory basis, Merger-related executive compensation arrangements. 8. To ratify the appointment of Ernst & Young LLP as Assertio’s independent registered public accounting firm for the fiscal year ending December 31, 2020. 9. To approve the adjournment from time to time of the Assertio Annual Meeting if necessary to solicit additional proxies if there are not sufficient votes to adopt the proposal to issue stock in connection with the Merger (Proposal 1) at the time of the Assertio Annual Meeting or any adjournment or postponement thereof. 10. To transact such other business as may properly come before the Assertio Annual Meeting and any adjournments or postponements thereof. Each of the foregoing items of business is more fully described in the Joint Proxy Statement/ Prospectus which is attached to and made part of this notice and which you are urged to read carefully. This Joint Proxy Statement/Prospectus and Assertio’s Annual Report on Form 10-K for fiscal year ended December 31, 2019 will be available electronically at https://www.cstproxy.com/assertiotx/2020. We cannot complete the Merger described in this Joint Proxy Statement/Prospectus unless the proposal to approve the issuance of shares of Assertio Holdings Common Stock is approved by a majority of the outstanding shares of common stock, $0.0001 par value per share, of Assertio present and entitled to vote on the proposal at the Assertio Annual Meeting.
Load more

Recommended publications
  • Companies in Attendance
    COMPANIES IN ATTENDANCE Abbott Diabetes Care Archbow Consulting LLC Business One Technologies Abbott Laboratories ARKRAY USA BusinessOneTech AbbVie Armory Hill Advocates, LLC CastiaRX ACADIA Artia Solutions Catalyst Acaria Health Asembia Celgene Accredo Assertio Therapeutics Celltrion Acer Therapeutics AssistRx Center for Creative Leadership Acorda Therapeutics Astellas Pharma US Inc. Cigna Actelion AstraZeneca Cigna Specialty Pharmacy AdhereTech Athenex Oncology Circassia Advantage Point Solutions Avanir Coeus Consulting Group Aerie Pharmaceuticals Avella Coherus Biosciences AGIOS AveXis Collaborative Associates LLC Aimmune Theraputics Bank of America Collegium Akcea Therapeutics Bausch Health Corsica Life Sciences Akebia Therapeutics Bayer U.S. CoverMyMeds Alder BioPharmaceuticals Becton Dickinson Creehan & Company, Inc., an Inovalon Company Alexion Biofrontera CSL Behring Alkermes Biogen Curant Health Allergan Biohaven CVS Health Almirall BioMarin D2 Consulting Alnylam BioMatrix Specialty Pharmacy Daiichi Sankyo Amarin BioPlus Specialty Pharmacy DBV Technologies Amber Pharmacy Bioventus Deloitte Consulting LLP AmerisourceBergen Blue Cross Blue Shield Association Dendreon Amgen Blue Fin Group Dermira Amicus Therapeutics bluebird bio Dexcom Amneal Boehringer Ingelheim Diplomat Pharmacy Anthem Boston Biomedical Dova Applied Policy Bowler and Company Decision Resources Group Aquestive Therapeutics Braeburn Eisai Arbor Pharmaceuticals Bristol-Myers Squibb 1 electroCore Indivior Merz Pharmaceuticals EMD Serono Inside Rx Milliman Encore Dermatology,
    [Show full text]
  • ASSERTIO THERAPEUTICS, INC. (Exact Name of Registrant As Specified in Its Charter) Delaware 94-3229046 (State Or Other Jurisdiction of (I.R.S
    UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 FORM 10-K (Mark one) ፤ ANNUAL REPORT PURSUANT TO SECTION 13 OR 15 (d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the fiscal year ended December 31, 2018 OR អ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 For the transition period from: to Commission File Number: 001-13111 ASSERTIO THERAPEUTICS, INC. (Exact Name of Registrant as Specified in its Charter) Delaware 94-3229046 (State or Other Jurisdiction of (I.R.S. Employer Incorporation or Organization) Identification No.) 100 South Saunders Road, Suite 300, Lake Forest, Illinois 60045 (Address of Principal Executive Offices) (Zip Code) Registrant’s telephone number, including area code: (224) 419-7106 Securities registered pursuant to Section 12(b) of the Act: Title of each class: Name of each exchange on which registered: Common Stock, $0.0001 par value The NASDAQ Stock Market LLC Securities registered pursuant to Section 12(g) of the Act: None Indicate by check mark if the registrant is a well-known seasoned issuer, as defined in Rule 405 of the Securities Act. Yes អ No ፤ Indicate by check mark if the registrant is not required to file reports pursuant to Section 13 or Section 15(d) of the Act. Yes អ No ፤ Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.
    [Show full text]
  • HIGHLIGHTSOF PRESCRIBING INFORMATION These Highlights Do
    HIGHLIGHTSOF PRESCRIBING INFORMATION • These highlights do not include all the information needed to use CAMBIA Hypertension: Patients taking some antihypertensive medications may safely and effectively. See full prescribing information for CAMBIA. have impaired response to these therapies when taking NSAIDs. Monitor blood pressure (5.4, 7) CAMBIA® (diclofenac potassium), for oral solution • Heart Failure and Edema: Avoid use of CAMBIA in patients with Initial U.S. Approval: 1988 severe heart failure unless benefits are expected to outweigh risk of worsening heart failure (5.5) WARNING: RISK OF SERIOUS CARDIOVASCULAR • Renal Toxicity: Monitor renal function in patients with renal or AND GASTROINTESTINAL EVENTS hepatic impairment, heart failure, dehydration, or hypovolemia. Avoid See full prescribing information for complete boxed warning use of CAMBIA in patients with advanced renal disease unless benefits are expected to outweigh risk of worsening renal function (5.6) Non-steroidal anti-inflammatory drugs (NSAIDs) cause an increased risk • Anaphylactic Reactions: Seek emergency help if an anaphylactic of serious cardiovascular thrombotic events, including myocardial reaction occurs (5.7) infarction and stroke, which can be fatal. This risk may occur early in treatment and may increase with duration of use (5.1) • Exacerbation of Asthma Related to Aspirin Sensitivity: CAMBIA is contraindicated in patients with aspirin-sensitive asthma. Monitor patients CAMBIA is contraindicated in the setting of coronary artery bypass with preexisting asthma (without aspirin sensitivity) (5.8) graft (CABG) surgery (4, 5.1) • Serious Skin Reactions: Discontinue CAMBIA at first appearance of skin rash or other signs of hypersensitivity (5.9). NSAIDs cause an increased risk of serious gastrointestinal (GI) adverse • Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS): events including bleeding, ulceration, and perforation of the stomach or Discontinue and evaluate clinically (5.10) intestines, which can be fatal.
    [Show full text]
  • ZIPSOR (Diclofenac Potassium) Capsules
    NDA 022202/S-013, S-014 SUPPLEMENT APPROVAL FULFILLMENT OF POSTMARKETING REQUIREMENT Assertio Therapeutics, Inc. 100 S. Saunders Road Suite 300 Lake Forest, IL 60045 Attention: Clorey Toombs, RAC Executive Director, Regulatory Affairs Dear Ms. Toombs: Please refer to your supplemental new drug applications (sNDA) dated and received November 9, 2018, (S-013) and November 17, 2020, (S-014) and your amendments, submitted under section 505(b) of the Federal Food, Drug, and Cosmetic Act (FDCA) for ZIPSOR (diclofenac potassium) capsules. Prior Approval supplement S-013 expands the approved indication for relief of mild to moderate acute pain in pediatric patients 12 years of age and older. We also refer to our letter dated October 15, 2020, notifying you, under Section 505(o)(4) of the FDCA, of new safety information that we believe should be included in the labeling for nonsteroidal anti-inflammatory drug (NSAID) products. This information pertains to the serious risks of fetal renal dysfunction, oligohydramnios, neonatal renal impairment, and Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS). Prior Approval supplement S-014 provides for safety labeling changes required under Section 505(o)(4) of the FDCA, consistent with our October 15, 2020, letter. APPROVAL & LABELING We have completed our review of these applications, as amended. They are approved, effective on the date of this letter, for use as recommended in the enclosed agreed- upon labeling. CONTENT OF LABELING As soon as possible, but no later than 14 days from the date of this letter, submit the content of labeling [21 CFR 314.50(l)] in structured product labeling (SPL) format using the FDA automated drug registration and listing system (eLIST), as described at Reference ID: 4799720 NDA 022202/S-013, S-014 Page 2 FDA.gov.1 Content of labeling must be identical to the enclosed labeling, with the addition of any labeling changes in pending “Changes Being Effected” (CBE) supplements, as well as annual reportable changes not included in the enclosed labeling.
    [Show full text]
  • Collegium Pharmaceutical Inc
    UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 FORM 8-K CURRENT REPORT Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 Date of Report (Date of earliest event reported): February 6, 2020 COLLEGIUM PHARMACEUTICAL, INC. (Exact name of registrant as specified in its charter) Virginia 001-37372 03-0416362 (state or other jurisdiction (Commission (I.R.S. Employer of incorporation) File Number) Identification No.) 100 Technology Center Drive Suite 300 Stoughton, MA 02072 (Address of principal executive offices) (Zip Code) Registrant’s telephone number, including area code: (781) 713-3699 (Former name or former address, if changed since last report) Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below): ¨ Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) ¨ Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) ¨ Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) ¨ Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) Indicated by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter). Emerging growth company ¨ If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.
    [Show full text]
  • IOA Two-Year Progress Report
    Two-Year Progress Report TABLE OF CONTENTS INTRODUCTION . 1 HISTORY OF THE IOA. 2 OPIOID BUSINESS RISKS: THE BUSINESS CASE FOR THE IOA . 5 IOA ENGAGEMENT STRATEGY AND COMPANIES . 8 KEY GOVERNANCE PROPOSALS FOR OPIOID SUPPLY CHAIN COMPANIES . 10 OPIOID BUSINESS RISKS BEYOND THE UNITED STATES . 17 APPENDIX 1 . 19 APPENDIX 2 . 20 APPENDIX 3 . 21 APPENDIX 4 . 22 APPENDIX 5 . 23 ENDNOTES . 27 INTRODUCTION This report summarizes the work of the Investors for • 26 negotiated settlements on governance issues Opioid Accountability (IOA) from July 1, 2017 to reached by companies and IOA members prior to a July 31, 2019. The IOA is a diverse global coalition vote of shareholders. of 57 members representing public, faith-based, labor, and sustainability funds, as well as investment • 4 negotiated settlements on governance issues managers, with $4 trillion in collective assets under reached by companies and IOA members following a management and advisement. The report covers the vote of shareholders. following topics: • 2 companies created a board level committee • The Business Case for the IOA; dedicated to oversight of opioids. • IOA Engagement Strategy & Companies; • 12 companies issued or committed to issue board risk reports. • Key Governance Proposals for Opioid Companies; • 10 companies adopted a misconduct clawback • Global Opioid Business Risks beyond the United policy. States; and • 3 companies agreed to separate the Chairman from • IOA Results by Company. CEO position. • 3 companies addressed executive compensation incentives by factoring in calculations of legal costs. Coalition Highlights by • 80 percent vote received for lobbying resolution filed the Numbers by IOA member United Church Funds at Mallinckrodt, • 57 members joined in fewer than two years.
    [Show full text]
  • Investment Portfolio 2019
    Teachers’ Retirement System of the City of New York Contents Introduction . .1 Statement of Total Investments for the Pension Fund . .3 Statement of Total Investments for the Diversified Equity Fund . .7 Statement of Total Investments for the Balanced Fund . .117 Statement of Total Investments for the International Equity Fund . .121 Statement of Total Investments for the Inflation Protection Fund . .161 Statement of Total Investments for the Socially Responsive Equity Fund . .165 Summary of Investment Managers . .169 Introduction The Teachers’ Retirement System of the City of New York (TRS) is pleased to present you with our Investment Portfolios publication for the fiscal year ended June 30, 2019. This publication lists the name and value of each investment that TRS held in its six investment programs at the closing of the fiscal year. Cash, receivables, and collateral from securities-lending transactions are assets of TRS but not of the investment programs; therefore, they are not included in this report. TRS’ investments as of June 30, 2019 are described briefly below: The Pension Fund consists of U.S. and international equities and fixed-income instruments, with smaller allocations made to private equity and real estate investments. It contains the City’s contributions toward TRS members’ retirement allowances (pension reserves) and members’ contributions to the Qualified Pension Plan (QPP). It also includes the assets of the Fixed Return Fund, an investment option for members that provides a fixed rate of return, determined by the New York State Legislature in accordance with applicable laws. The Diversified Equity Fund invests primarily in the stocks of U.S.
    [Show full text]
  • Antibe Therapeutics ATE-TSXV: $0.29 White Paper on ATB-346 Phase II Performance Affirms Our Speculative BUY Positive View on Drug Potential – Spec BUY $1.40 Target
    29 August 2018 Healthcare & Biotechnology Antibe Therapeutics ATE-TSXV: $0.29 White Paper On ATB-346 Phase II Performance Affirms Our Speculative BUY Positive View On Drug Potential – Spec BUY $1.40 Target Event: ON-based drug developer Antibe Therapeutics posted a white paper on its website Projected Return: 383% yesterday that provides added granularity on data derived from its completed 244-patient Valuation: NPV, 20x EPS, 12.5x Phase II gastroduodenal ulceration rate trial, comparing its hydrogen sulfide-releasing EV/EBITDA naproxen analog drug ATB-346 to naproxen itself at doses at which naproxen is, and ATB-346 (F2025 estimates, 40% discount rate) is predicted to, confer measurable symptomatic relief in knee osteoarthritis pain. In parallel, Antibe reported FQ119 financial data for the June-end quarter this morning, data that is less impactful on our valuation than ATB-346 development activities, but we will provide relevant commentary below. Bottom line: Our fundamental investment thesis on Antibe’s pipeline of hydrogen sulfide- releasing pain therapies, and specifically of cyclooxygenase-1-inhibiting non-steroidal anti- inflammatory drugs (NSAIDs) for which GI ulceration is a recognized side effect, is unchanged and we remain positive on how the firm’s lead drug ATB-346 performed in recent Phase II GI ulceration rate testing and could subsequently perform in pending Phase II knee osteoarthritis pain testing, for which we expect final pain data by FQ120 (CQ219). We are maintaining our Speculative BUY rating and PT of $1.40 on ATE, with our valuation still based on NPV (40% discount rate that will become increasingly conservative as ATB-346 advances through Phase II testing) and multiples of our F2025 adjusted EBITDA/fd EPS forecasts ($165.6M/$0.41, respectively).
    [Show full text]
  • Appendix B - Product Name Sorted by Applicant
    JUNE 2021 - APPROVED DRUG PRODUCT LIST B - 1 APPENDIX B - PRODUCT NAME SORTED BY APPLICANT ** 3 ** 3D IMAGING DRUG * 3D IMAGING DRUG DESIGN AND DEVELOPMENT LLC AMMONIA N 13, AMMONIA N-13 FLUDEOXYGLUCOSE F18, FLUDEOXYGLUCOSE F-18 SODIUM FLUORIDE F-18, SODIUM FLUORIDE F-18 3M * 3M CO PERIDEX, CHLORHEXIDINE GLUCONATE * 3M HEALTH CARE INC AVAGARD, ALCOHOL (OTC) DURAPREP, IODINE POVACRYLEX (OTC) 3M HEALTH CARE * 3M HEALTH CARE INFECTION PREVENTION DIV SOLUPREP, CHLORHEXIDINE GLUCONATE (OTC) ** 6 ** 60 DEGREES PHARMS * 60 DEGREES PHARMACEUTICALS LLC ARAKODA, TAFENOQUINE SUCCINATE ** A ** AAA USA INC * ADVANCED ACCELERATOR APPLICATIONS USA INC LUTATHERA, LUTETIUM DOTATATE LU-177 NETSPOT, GALLIUM DOTATATE GA-68 AAIPHARMA LLC * AAIPHARMA LLC AZASAN, AZATHIOPRINE ABBVIE * ABBVIE INC ANDROGEL, TESTOSTERONE CYCLOSPORINE, CYCLOSPORINE DEPAKOTE ER, DIVALPROEX SODIUM DEPAKOTE, DIVALPROEX SODIUM GENGRAF, CYCLOSPORINE K-TAB, POTASSIUM CHLORIDE KALETRA, LOPINAVIR NIASPAN, NIACIN NIMBEX PRESERVATIVE FREE, CISATRACURIUM BESYLATE NIMBEX, CISATRACURIUM BESYLATE NORVIR, RITONAVIR SYNTHROID, LEVOTHYROXINE SODIUM ** TARKA, TRANDOLAPRIL TRICOR, FENOFIBRATE TRILIPIX, CHOLINE FENOFIBRATE ULTANE, SEVOFLURANE ZEMPLAR, PARICALCITOL ABBVIE ENDOCRINE * ABBVIE ENDOCRINE INC LUPANETA PACK, LEUPROLIDE ACETATE ABBVIE ENDOCRINE INC * ABBVIE ENDOCRINE INC LUPRON DEPOT, LEUPROLIDE ACETATE LUPRON DEPOT-PED KIT, LEUPROLIDE ACETATE ABBVIE INC * ABBVIE INC DUOPA, CARBIDOPA MAVYRET, GLECAPREVIR NORVIR, RITONAVIR ORIAHNN (COPACKAGED), ELAGOLIX SODIUM,ESTRADIOL,NORETHINDRONE ACETATE
    [Show full text]
  • Drug Formulary
    Drug Formulary Manufacturer: Medication: Manufacturer: Medication: ABBVIE Androgel ASSERTIO THERAPEUTICS Cambria ABBVIE Creon ASSERTIO THERAPEUTICS Gralise ABBVIE Humira ASSERTIO THERAPEUTICS Nucynta ER ADAPT PHARMA Narcan ASSERTIO THERAPEUTICS Zipsor AKORN Azasite ASTELLAS Myrbetriq AKORN Cosopt ASTELLAS Vesicare ALFASIGMA USA Cerefolin ASTRAZENECA Bevespi ALFASIGMA USA Deplin ASTRAZENECA Byduron ALFASIGMA USA Metanx ASTRAZENECA Daliresp ALLERGAN Acuvail ASTRAZENECA Farxiga ALLERGAN Alphagam ASTRAZENECA Movantik ALLERGAN Androderm ASTRAZENECA Tudorza ALLERGAN Bystolic ASTRAZENECA LP Brilanta ALLERGAN Combigan ASTRAZENECA LP Pulmicort ALLERGAN Delzicol ASTRAZENECA LP Symbicort ALLERGAN Fetzima AVANIR PHARMACEUTICALS, LLC Nuedexta ALLERGAN Gelnique AVANIR PHARMACEUTICALS, LLC Onzetra ALLERGAN Lastacaft BAUSCH HEALTH Alrex ALLERGAN Linzess BAUSCH HEALTH Aplenzin ALLERGAN Lumigan BAUSCH HEALTH Ativan ALLERGAN Namenda XR BAUSCH HEALTH Besivance ALLERGAN Namzaric BAUSCH HEALTH Elidel ALLERGAN Pylera BAUSCH HEALTH Istalol ALLERGAN Rapaflo BAUSCH HEALTH Lotemax ALLERGAN Savella BAUSCH HEALTH Luzu ALLERGAN Viberzi BAUSCH HEALTH Prolenza ALLERGAN Viibyrd BAUSCH HEALTH Relistor ALMATICA Napelan BAUSCH HEALTH Trulance AMARIN PHARMA Vascepa BAUSCH HEALTH Wellbutrin XL AMGEN Corlanor BIODELIVERY SCIENCES Belbuca AMGEN Repatha BIODELIVERY SCIENCES Bunavil AMNEAL SPECIALTY Zomig BIOVENTUS Supartz ANTARES PHARMA Otrexup B-M SQUIBB U.S. (PRIMARY CARE) Coumadin ARBOR PHARMACEUTICALS Edarbi B-M SQUIBB U.S. (PRIMARY CARE) Eliquis ARBOR PHARMACEUTICALS Edarbyclor
    [Show full text]
  • MED-Project Participating Drug Companies - King County Washington, March 2020
    MED-Project Participating Drug Companies - King County Washington, March 2020 Drug Company Name Parent Company 3M Corporation 3M Corporation 3M Drug Delivery Systems 3M Corporation 3M ESPE 3M Corporation 3M Health Care 3M Corporation 3M Personal Care 3M Corporation AbbVie Inc. AbbVie Inc. ACADIA Pharmaceuticals Inc. ACADIA Pharmaceuticals Inc. Accord Healthcare Inc. Accord Healthcare Inc. Acorda Therapeutics, Inc. Acorda Therapeutics, Inc. Acorda Therapeutics, Inc. Acorda Therapeutics, Inc. Actavis Generics Teva Pharmaceuticals USA, Inc. Actavis Pharma, Inc. (only for labeler code 52544) Allergan, Inc. Actelion Johnson & Johnson Adapt Pharma Inc. Adapt Pharma Inc. Advanced Vision Research Inc. d.b.a. Akorn Consumer Health Akorn, Inc. Advantice Health Advantice Health Aegerion Pharmaceuticals, Inc. Aegerion Pharmaceuticals, Inc. Afaxys Inc. Afaxys Inc. Afaxys Pharmaceuticals (a division of Afaxys Inc.) Afaxys Inc. Affordable Pharmaceuticals LLC Sebela Pharmaceuticals Inc. Ajanta Pharma USA Inc. Ajanta Pharma USA Inc. AkaRx, Inc., dba Dova Pharmaceuticals AkaRx, Inc., dba Dova Pharmaceuticals Akebia Therapeutics, Inc. Akebia Therapeutics, Inc. Akorn Animal Health, Inc. Akorn, Inc. Akorn, Inc. Akorn, Inc. Akrimax Pharmaceuticals, LLC Akrimax Pharmaceuticals, LLC AKRON COATING & ADHESIVES AKRON COATING & ADHESIVES Alaven Pharmaceuticals LLC Mylan Inc. Alcon Laboratories, Inc. Novartis Group Companies Alembic Pharmaceuticals Inc. Alembic Pharmaceuticals Inc. Allergan Sales, LLC Allergan, Inc. Allergan USA, Inc. Allergan, Inc. Allergan, Inc. Allergan, Inc. Almaject, Inc. Alvogen Pharma US, Inc. Almatica Pharma, Inc. Alvogen Pharma US, Inc. Almirall LLC Almirall LLC Alphapharm Pty Ltd Mylan Inc. Alva-Amco Pharmacal Companies, Inc. Alva-Amco Pharmacal Companies, Inc. Alvogen Pharma US, Inc. Alvogen Pharma US, Inc. Alvogen, Inc. Alvogen Pharma US, Inc. AMAG Pharma USA, Inc.
    [Show full text]
  • Form 10-K Assertio Therapeutics, Inc
    UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 FORM 10-K x ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 FOR THE FISCAL YEAR ENDED December 31, 2019 OR ¨ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 FOR THE TRANSITION PERIOD FROM TO Commission File Number: 001‑13111 ASSERTIO THERAPEUTICS, INC. (Exact Name of Registrant as Specified in its Charter) Delaware 94‑3229046 (State or Other Jurisdiction of (I.R.S. Employer Incorporation or Organization) Identification No.) 100 South Saunders Road, Suite 300, Lake Forest, Illinois 60045 (Address of Principal Executive Offices) (Zip Code) Registrant’s telephone number, including area code: (224) 419‑7106 Securities registered pursuant to Section 12(b) of the Act: Title of each class: Trading Symbol(s): Name of each exchange on which registered: Common Stock, $0.0001 par value ASRT The Nasdaq Stock Market LLC Securities registered pursuant to Section 12(g) of the Act: None Indicate by check mark if the registrant is a well‑known seasoned issuer, as defined in Rule 405 of the Securities Act. Yes ¨ No ý Indicate by check mark if the registrant is not required to file reports pursuant to Section 13 or Section 15(d) of the Act. Yes ¨ No ý Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.
    [Show full text]