Active Ingredient: HYDROCHLOROTHIAZIDE; PROPRANOLOL HYDROCHLORIDE
Proprietary Name: PROPRANOLOL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG;40MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A071771
Product Number: 001
Approval Date: Jan 26, 1988
Applicant Holder Full Name: WARNER CHILCOTT DIV WARNER LAMBERT CO
Marketing Status:
Discontinued
Patent and Exclusivity Information
