FDA NDC Directory · JSON-LD · Markdown
NDC 72338-200 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
| Generic name | bortezomib |
|---|---|
| Labeler / Manufacturer | Waverley Pharma Inc |
| Marketing category | Abbreviated NDA (generic) · App ANDA211898 |
| Dosage form / route | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS SUBCUTANEOUS |
| Active ingredients | BORTEZOMIB (3.5 mg/1) |
| Marketing started | 20180619 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).