FDA NDC Directory · JSON-LD · Markdown
NDC 24338-270 · HUMAN PRESCRIPTION DRUG · INJECTION
| Generic name | BENDAMUSTINE HYDROCHLORIDE |
|---|---|
| Labeler / Manufacturer | Azurity Pharmaceuticals, Inc. |
| Marketing category | New Drug Application (innovator) · App NDA212209 |
| Dosage form / route | INJECTION · INTRAVENOUS |
| Active ingredients | BENDAMUSTINE HYDROCHLORIDE (25 mg/mL) |
| Marketing started | 20250401 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).