FDA NDC Directory · JSON-LD · Markdown
NDC 0143-9568 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION
| Labeler / Manufacturer | Hikma Pharmaceuticals USA Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA065048 |
| Dosage form / route | INJECTION, POWDER, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS |
| Active ingredients | CEFUROXIME SODIUM (750 mg/1) |
| Marketing started | 20040109 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).