Active Ingredient: PROPRANOLOL HYDROCHLORIDE
Proprietary Name: PROPRANOLOL HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 40MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A070142
Product Number: 001
Approval Date: Jul 30, 1985
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information