Generated: November 18, 2017
DrugPatentWatch Database Preview
Details for New Drug Application (NDA): 070321
describes PROPRANOLOL HYDROCHLORIDE
, which is a drug marketed by Inwood Labs, Sandoz Inc, Rp Scherer, Anda Repository, Duramed Pharms Barr, Upsher-smith Labs, Mylan, Northstar Hlthcare, Purepac Pharm, Superpharm, Roxane, Lederle, Vintage Pharms, Baxter Hlthcare Corp, Schering, Zydus Pharms Usa Inc, Dava Pharms Inc, Fresenius Kabi Usa, Teva, Smith And Nephew, Solopak, Warner Chilcott, Watson Labs, Watson Labs Teva, Ipca Labs Ltd, Sandoz, Hikma Farmaceutica, Ivax Sub Teva Pharms, Nortec Dev Assoc, Interpharm, Impax Labs Inc, Ani Pharms Inc, West-ward Pharms Int, Morton Grove, Par Pharm, Athenex Inc, and Actavis Elizabeth, and is included in one hundred and forty-nine NDAs. It is available from fifty-one suppliers. Additional details are available on the PROPRANOLOL HYDROCHLORIDE profile page.
The generic ingredient in PROPRANOLOL HYDROCHLORIDE is hydrochlorothiazide; propranolol hydrochloride. There are thirty-one 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.
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Summary for product number 001
|Approval Date:||Sep 24, 1986||TE:||RLD:||No|
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