FDA NDC Directory · JSON-LD · Markdown
NDC 0003-0371 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
| Generic name | BELATACEPT |
|---|---|
| Labeler / Manufacturer | E.R. Squibb & Sons, L.L.C. |
| Marketing category | Biologic License Application · App BLA125288 |
| Dosage form / route | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS |
| Active ingredients | BELATACEPT (250 mg/1) |
| Marketing started | 20110615 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).