Active Ingredient: PROPRANOLOL HYDROCHLORIDE
Proprietary Name: PROPRANOLOL HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 60MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A070441
Product Number: 001
Approval Date: Sep 24, 1986
Applicant Holder Full Name: WARNER CHILCOTT INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
