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Vancomycin Hydrochloride

NDC 39822-0470 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerXGen Pharmaceuticals DJB, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA215324
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsVANCOMYCIN HYDROCHLORIDE (1.5 g/1)
Marketing started20251215
Package count1

External sources

Source: openFDA. Public-domain (CC0).