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Vancomycin Hydrochloride

NDC 0143-9152 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217489
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsVANCOMYCIN HYDROCHLORIDE (1.25 g/1)
Marketing started20230717
Package count1

External sources

Source: openFDA. Public-domain (CC0).