FDA NDC Directory · JSON-LD · Markdown

Aminocaproic acid

NDC 0904-7165 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA212492
Dosage form / routeTABLET · ORAL
Active ingredientsAMINOCAPROIC ACID (500 mg/1)
Marketing started20191130
Package count1

External sources

Source: openFDA. Public-domain (CC0).