FDA NDC Directory · JSON-LD · Markdown
NDC 72205-286 · HUMAN PRESCRIPTION DRUG · TABLET
| Labeler / Manufacturer | Novadoz Pharmaceuticals LLC |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA212938 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | AMINOCAPROIC ACID (1000 mg/1) |
| Marketing started | 20230913 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).