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: A070817
Product Number: 001
Approval Date: Nov 3, 1986
Applicant Holder Full Name: PUREPAC PHARMACEUTICAL CO
Marketing Status:
Discontinued
Patent and Exclusivity Information