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Micafungin

NDC 70710-1725 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA215241
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsMICAFUNGIN SODIUM (20 mg/mL)
Marketing started20230410
Package count2

External sources

Source: openFDA. Public-domain (CC0).