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Generated: December 15, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 071771

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NDA 071771 describes PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE, which is a drug marketed by Actavis Elizabeth, Ani Pharms Inc, Ivax Sub Teva Pharms, Mylan, Sandoz, Warner Chilcott, and Watson Labs, 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 071771

Tradename:1
Applicant:1
Ingredient:1
Patents:0
Formulation / Manufacturing:see details

Summary for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength25MG;40MG
Approval Date:Jan 26, 1988TE:RLD:No


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Colorcon
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McKinsey
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Dow

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