FDA NDC Directory · JSON-LD · Markdown

AMINOCAPROIC ACID

NDC 70377-102 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerBiocon Pharma Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213928
Dosage form / routeTABLET · ORAL
Active ingredientsAMINOCAPROIC ACID (500 mg/1)
Marketing started20210315
Package count1

External sources

Source: openFDA. Public-domain (CC0).