FDA NDC Directory · JSON-LD · Markdown
NDC 57894-350 · HUMAN PRESCRIPTION DRUG · SOLUTION
| Generic name | golimumab |
|---|---|
| Labeler / Manufacturer | Janssen Biotech, Inc. |
| Marketing category | Biologic License Application · App BLA125433 |
| Dosage form / route | SOLUTION · INTRAVENOUS |
| Active ingredients | GOLIMUMAB (50 mg/4mL) |
| Marketing started | 20130719 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).