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Vancomycin Hydrochloride

NDC 68462-958 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerGLENMARK PHARMACEUTICALS INC., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA205694
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsVANCOMYCIN HYDROCHLORIDE (10 g/100mL)
Marketing started20261012
Package count1

External sources

Source: openFDA. Public-domain (CC0).