FDA NDC Directory · JSON-LD · Markdown

Valacyclovir

NDC 69117-0010 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerYiling Pharmaceutical, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209553
Dosage form / routeTABLET · ORAL
Active ingredientsVALACYCLOVIR HYDROCHLORIDE (500 mg/1)
Marketing started20181001
Package count3

External sources

Source: openFDA. Public-domain (CC0).