FDA NDC Directory · JSON-LD · Markdown
NDC 63459-348 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION
| Generic name | bendamustine hydrochloride |
|---|---|
| Labeler / Manufacturer | Teva Pharmaceuticals USA, Inc. |
| Marketing category | New Drug Application (innovator) · App NDA208194 |
| Dosage form / route | INJECTION, SOLUTION · INTRAVENOUS |
| Active ingredients | BENDAMUSTINE HYDROCHLORIDE (25 mg/mL) |
| Marketing started | 20151208 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).