FDA NDC Directory · JSON-LD · Markdown
NDC 84976-001 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
| Generic name | tividenofusp alfa-eknm |
|---|---|
| Labeler / Manufacturer | Denali Therapeutics Inc. |
| Marketing category | Biologic License Application · App BLA761485 |
| Dosage form / route | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS |
| Active ingredients | TIVIDENOFUSP ALFA (150 mg/5mL) |
| Marketing started | 20260406 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).