Active Ingredient: ATENOLOL
Proprietary Name: ATENOLOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A073318
Product Number: 001
Approval Date: Mar 20, 1992
Applicant Holder Full Name: APOTHECON SUB BRISTOL MYERS SQUIBB CO
Marketing Status:
Discontinued
Patent and Exclusivity Information