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Serving hundreds of leading biopharmaceutical companies globally:

McKinsey
Fish and Richardson
McKesson
Express Scripts
US Department of Justice
Federal Trade Commission
Merck
UBS
Citi

Generated: May 26, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 074723

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NDA 074723 describes DICLOFENAC SODIUM, which is a drug marketed by Actavis Mid Atlantic, Amneal Pharms, Glenmark Pharms Ltd, Taro, Tolmar, Akorn, Altaire Pharms Inc, Apotex Inc, Bausch And Lomb, Falcon Pharms, Rising Pharms Inc, Sandoz Inc, Anda Repository, Lupin Ltd, Novel Labs Inc, Riconpharma Llc, Teligent Pharma Inc, Watson Labs Inc, Zydus Pharms Usa Inc, Actavis Elizabeth, Allied Pharma Inc, Carlsbad, Casi Pharms Inc, Mylan Pharms Inc, Pliva, Roxane, Teva, Teva Pharms, Unique Pharm Labs, Dexcel Ltd, Mylan, Vpna, Actavis Labs Fl Inc, Exela Holdings, and Sandoz, and is included in forty-three NDAs. It is available from seventy-seven suppliers. Additional details are available on the DICLOFENAC SODIUM profile page.

The generic ingredient in DICLOFENAC SODIUM is diclofenac sodium; misoprostol. There are forty-seven drug master file entries for this compound. Seventeen suppliers are listed for this compound. Additional details are available on the diclofenac sodium; misoprostol profile page.
Summary for 074723
Tradename:DICLOFENAC SODIUM
Applicant:Teva
Ingredient:diclofenac sodium
Patents:0
Therapeutic Class:Analgesics
Anti-inflammatory Agents
Dermatological Agents
Ophthalmic Agents
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET, DELAYED RELEASE;ORALStrength50MG
Approval Date:Mar 30, 1999TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Harvard Business School
Mallinckrodt
Covington
Federal Trade Commission
UBS
QuintilesIMS
Argus Health
Boehringer Ingelheim
Fuji

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