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Vancomycin Hydrochloride

NDC 68001-407 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA204125
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsVANCOMYCIN HYDROCHLORIDE (10 g/1)
Marketing started20190823
Package count1

External sources

Source: openFDA. Public-domain (CC0).