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VANCOMYCIN HYDROCHLORIDE

NDC 70436-020 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerSlate Run Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212332
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsVANCOMYCIN HYDROCHLORIDE (500 mg/1)
Marketing started20190603
Package count1

External sources

Source: openFDA. Public-domain (CC0).