FDA NDC Directory · JSON-LD · Markdown
NDC 0143-9270 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
| Labeler / Manufacturer | Hikma Pharmaceuticals USA Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA075387 |
| Dosage form / route | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRA-ARTERIAL |
| Active ingredients | FLOXURIDINE (100 mg/mL) |
| Marketing started | 20180215 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).