FDA NDC Directory · JSON-LD · Markdown

Valsartan

NDC 55111-734 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerDr. Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA201618
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVALSARTAN (320 mg/1)
Marketing started20180119
Package count5

External sources

Source: openFDA. Public-domain (CC0).