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Valacyclovir

NDC 61919-066 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerDirect Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA201506
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVALACYCLOVIR HYDROCHLORIDE (500 mg/1)
Marketing started20150101
Package count2

External sources

Source: openFDA. Public-domain (CC0).