FDA NDC Directory · JSON-LD · Markdown
NDC 63323-321 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
| Generic name | POLYMYXIN B SULFATE |
|---|---|
| Labeler / Manufacturer | Fresenius Kabi USA, LLC |
| Marketing category | Abbreviated NDA (generic) · App ANDA065372 |
| Dosage form / route | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAMUSCULAR INTRATHECAL INTRAVENOUS OPHTHALMIC |
| Active ingredients | POLYMYXIN B SULFATE (500000 [USP'U]/1) |
| Marketing started | 20091117 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).