FDA NDC Directory · JSON-LD · Markdown
NDC 0904-7399 · HUMAN PRESCRIPTION DRUG · TABLET
| Labeler / Manufacturer | MAJOR PHARMACEUTICALS |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA208256 |
| Dosage form / route | TABLET · ORAL |
| Active ingredients | ROFLUMILAST (500 ug/1) |
| Marketing started | 20231226 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).