Active Ingredient: ATENOLOL
Proprietary Name: ATENOLOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A073026
Product Number: 001
Approval Date: Sep 17, 1991
Applicant Holder Full Name: HEALTHCARE PHARMACEUTICALS LTD
Marketing Status:
Prescription
Patent and Exclusivity Information