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Ganciclovir

NDC 42023-173 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerEndo USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204950
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsGANCICLOVIR SODIUM (500 mg/10mL)
Marketing started20161206
Package count1

External sources

Source: openFDA. Public-domain (CC0).