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: A070122
Product Number: 001
Approval Date: Aug 6, 1985
Applicant Holder Full Name: SCHERING CORP SUB SCHERING PLOUGH CORP
Marketing Status:
Discontinued
Patent and Exclusivity Information