FDA NDC Directory · JSON-LD · Markdown
NDC 51144-030 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
| Generic name | ENFORTUMAB VEDOTIN |
|---|---|
| Labeler / Manufacturer | SEAGEN INC. |
| Marketing category | Biologic License Application · App BLA761137 |
| Dosage form / route | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS |
| Active ingredients | ENFORTUMAB VEDOTIN (30 mg/3mL) |
| Marketing started | 20191218 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).