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Serving hundreds of leading biopharmaceutical companies globally:

Fuji
McKesson
Cipla
Farmers Insurance
Healthtrust
Fish and Richardson
Merck
Chubb
Accenture

Generated: June 19, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 070122

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NDA 070122 describes PROPRANOLOL HYDROCHLORIDE, which is a drug marketed by Actavis Elizabeth, Inwood Labs, Mylan, Nortec Dev Assoc, Rp Scherer, Upsher-smith Labs, Zydus Pharms Usa Inc, Athenex Inc, Baxter Hlthcare Corp, Fosun Pharma, Fresenius Kabi Usa, Hikma Farmaceutica, Smith And Nephew, Solopak, Morton Grove, West-ward Pharms Int, Anda Repository, Ani Pharms Inc, Dava Pharms Inc, Duramed Pharms Barr, Impax Labs Inc, Interpharm, Ipca Labs Ltd, Ivax Sub Teva Pharms, Lederle, Northstar Hlthcare, Par Pharm, Purepac Pharm, Roxane, Sandoz, Schering, Superpharm, Teva, Vintage Pharms, Warner Chilcott, Watson Labs, Watson Labs Teva, and Yaopharma Co Ltd, and is included in one hundred and forty-three NDAs. It is available from fifty suppliers. Additional details are available on the PROPRANOLOL HYDROCHLORIDE profile page.

The generic ingredient in PROPRANOLOL HYDROCHLORIDE is hydrochlorothiazide; propranolol hydrochloride. There are thirty-two drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the hydrochlorothiazide; propranolol hydrochloride profile page.
Summary for 070122
Tradename:PROPRANOLOL HYDROCHLORIDE
Applicant:Schering
Ingredient:propranolol hydrochloride
Patents:0
Therapeutic Class:Antimigraine Agents
Cardiovascular Agents
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength40MG
Approval Date:Aug 6, 1985TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Deloitte
Federal Trade Commission
Cantor Fitzgerald
Johnson and Johnson
McKinsey
Boehringer Ingelheim
Mallinckrodt
Baxter
Medtronic

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