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Valacyclovir Hydrochloride

NDC 68084-309 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA090682
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVALACYCLOVIR HYDROCHLORIDE (1 g/1)
Marketing started20140306
Package count1

External sources

Source: openFDA. Public-domain (CC0).