FDA NDC Directory · JSON-LD · Markdown

Valacyclovir hydrochloride

NDC 68788-6896 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077135
Dosage form / routeTABLET · ORAL
Active ingredientsVALACYCLOVIR HYDROCHLORIDE (500 mg/1)
Marketing started20170213
Package count6

External sources

Source: openFDA. Public-domain (CC0).