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Serving hundreds of leading biopharmaceutical companies globally:

US Department of Justice
Fuji
Cantor Fitzgerald
Merck
Harvard Business School
Colorcon
Julphar
Teva
Citi

Generated: April 24, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 077855

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NDA 077855 describes MORPHINE SULFATE, which is a drug marketed by Actavis Elizabeth, Impax Labs Inc, Par Pharm Inc, Teva Pharms Usa, Upsher-smith Labs, Eurohlth Intl Sarl, Hospira, Hospira Inc, Icu Medical Inc, Meridian Medcl Techn, Specgx Llc, Watson Labs, Fresenius Kabi Usa, Hi-tech Pharmacal, Lannett Holdings Inc, Nostrum Labs Inc, Paddock Llc, Pharm Assoc, Rhodes Pharms, Tris Pharma Inc, Vintage Pharms Llc, Vistapharm, West-ward Pharms Int, Dava Pharms Inc, Epic Pharma Llc, Mayne Pharma Inc, Mylan Pharms Inc, Nesher Pharms, Novel Labs Inc, Sun Pharm Inds Ltd, and Sun Pharm Industries, and is included in fifty-three NDAs. It is available from forty-three suppliers. There are three patents protecting this drug. Additional details are available on the MORPHINE SULFATE profile page.

The generic ingredient in MORPHINE SULFATE is morphine sulfate. There are twenty-three drug master file entries for this compound. Forty-nine suppliers are listed for this compound. Additional details are available on the morphine sulfate profile page.
Summary for 077855
Tradename:MORPHINE SULFATE
Applicant:Nesher Pharms
Ingredient:morphine sulfate
Patents:0
Therapeutic Class:Analgesics
Formulation / Manufacturing:see details
Pharmacology for NDA: 077855
Mechanism of ActionFull Opioid Agonists
Medical Subject Heading (MeSH) Categories for 077855
Suppliers and Packaging for NDA: 077855
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
MORPHINE SULFATE morphine sulfate TABLET, EXTENDED RELEASE;ORAL 077855 ANDA Zydus Pharmaceuticals (USA) Inc. 68382-906 N 68382-906-01
MORPHINE SULFATE morphine sulfate TABLET, EXTENDED RELEASE;ORAL 077855 ANDA Zydus Pharmaceuticals (USA) Inc. 68382-907 N 68382-907-01

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET, EXTENDED RELEASE;ORALStrength100MG
Approval Date:Sep 27, 2007TE:ABRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:TABLET, EXTENDED RELEASE;ORALStrength200MG
Approval Date:Sep 27, 2007TE:ABRLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Farmers Insurance
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Federal Trade Commission
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Queensland Health
Healthtrust
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Express Scripts
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