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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: A212492
Product Number: 001
Approval Date: Nov 26, 2019
Applicant Holder Full Name: AMNEAL EU LTD
Marketing Status:
Prescription
Patent and Exclusivity Information