FDA NDC Directory · JSON-LD · Markdown
NDC 63323-342 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION
| Generic name | Cefoxitin Sodium |
|---|---|
| Labeler / Manufacturer | Fresenius Kabi USA, LLC |
| Marketing category | Abbreviated NDA (generic) · App ANDA065414 |
| Dosage form / route | POWDER, FOR SOLUTION · INTRAVENOUS |
| Active ingredients | CEFOXITIN SODIUM (2 g/1) |
| Marketing started | 20110706 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).