FDA NDC Directory · JSON-LD · Markdown
NDC 65219-200 · HUMAN PRESCRIPTION DRUG · KIT
| Labeler / Manufacturer | Fresenius Kabi USA, LLC |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA207383 |
| Dosage form / route | KIT · INTRAVENOUS |
| Active ingredients | — |
| Marketing started | 20201120 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).