Active Ingredient: ENALAPRILAT
Proprietary Name: ENALAPRILAT
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 1.25MG/ML
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AP
Application Number: A078687
Product Number: 001
Approval Date: Dec 23, 2008
Applicant Holder Full Name: HIKMA FARMACEUTICA (PORTUGAL) SA
Marketing Status:
Prescription
Patent and Exclusivity Information
