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Details for New Drug Application (NDA): 070301

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NDA 070301 describes PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE, which is a drug marketed by Watson Labs, Ani Pharms Inc, Mylan, Actavis Elizabeth, Ivax Sub Teva Pharms, Sandoz, and Warner Chilcott, and is included in seventeen NDAs. It is available from one supplier. Additional details are available on the PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE profile page.

The generic ingredient in PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE 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.

Summary for NDA: 070301

Summary for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength25MG;40MG
Approval Date:Apr 18, 1986TE:RLD:No


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