Details for New Drug Application (NDA): 070851
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The generic ingredient in PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE is hydrochlorothiazide; propranolol hydrochloride. There are thirty-two drug master file entries for this compound. Additional details are available on the hydrochlorothiazide; propranolol hydrochloride profile page.
Summary for 070851
Tradename: | PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE |
Applicant: | Actavis Elizabeth |
Ingredient: | hydrochlorothiazide; propranolol hydrochloride |
Patents: | 0 |
Profile for product number 001
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 25MG;40MG | ||||
Approval Date: | May 15, 1986 | TE: | RLD: | No |
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