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Valacyclovir Hydrochloride

NDC 51655-633 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090682
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVALACYCLOVIR HYDROCHLORIDE (500 mg/1)
Marketing started20230105
Package count2

External sources

Source: openFDA. Public-domain (CC0).