FDA NDC Directory · JSON-LD · Markdown

Aminocaproic acid

NDC 72205-049 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNovadoz Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212938
Dosage form / routeTABLET · ORAL
Active ingredientsAMINOCAPROIC ACID (500 mg/1)
Marketing started20201210
Package count1

External sources

Source: openFDA. Public-domain (CC0).