FDA NDC Directory · JSON-LD · Markdown
NDC 76420-151 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED
| Labeler / Manufacturer | Asclemed USA, Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA203687 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | FINASTERIDE (1 mg/1) |
| Marketing started | 20131105 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).