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Micafungin

NDC 42658-022 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, FOR SOLUTION

Labeler / ManufacturerHisun Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA219712
Dosage form / routeINJECTION, POWDER, FOR SOLUTION · INTRAVENOUS
Active ingredientsMICAFUNGIN SODIUM (50 mg/1)
Marketing started20260401
Package count2

External sources

Source: openFDA. Public-domain (CC0).