FDA NDC Directory · JSON-LD · Markdown
NDC 63323-030 · HUMAN PRESCRIPTION DRUG · KIT
| Labeler / Manufacturer | Fresenius Kabi USA, LLC |
|---|---|
| Marketing category | Biologic License Application · App BLA017067 |
| Dosage form / route | KIT |
| Active ingredients | — |
| Marketing started | 20110421 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).