FDA NDC Directory · JSON-LD · Markdown
NDC 71655-578 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
| Generic name | Ansuvimab |
|---|---|
| Labeler / Manufacturer | Emergent Manufacturing Operations Baltimore, LLC |
| Marketing category | Biologic License Application · App BLA761172 |
| Dosage form / route | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS |
| Active ingredients | ANSUVIMAB (400 mg/8mL) |
| Marketing started | 20201221 |
| Package count | 3 |
Source: openFDA. Public-domain (CC0).