Active Ingredient: AMINOCAPROIC ACID
Proprietary Name: AMINOCAPROIC ACID
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 500MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A213928
Product Number: 001
Approval Date: Feb 12, 2021
Applicant Holder Full Name: CARNEGIE PHARMACEUTICALS LLC
Marketing Status:
Prescription
Patent and Exclusivity Information