FDA NDC Directory · JSON-LD · Markdown
NDC 70710-1724 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
| Labeler / Manufacturer | Zydus Pharmaceuticals USA Inc. |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA215241 |
| Dosage form / route | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS |
| Active ingredients | MICAFUNGIN SODIUM (10 mg/mL) |
| Marketing started | 20230410 |
| Package count | 2 |
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