FDA NDC Directory · JSON-LD · Markdown
NDC 60505-6236 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
| Labeler / Manufacturer | Apotex Corp. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA207384 |
| Dosage form / route | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS |
| Active ingredients | DEFEROXAMINE MESYLATE (500 mg/1) |
| Marketing started | 20211105 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).