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Valacyclovir Hydrochloride

NDC 76420-459 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerASCLEMED USA INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA090682
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVALACYCLOVIR HYDROCHLORIDE (500 mg/1)
Marketing started20100524
Package count12

External sources

Source: openFDA. Public-domain (CC0).