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Valsartan

NDC 55111-732 · 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 (80 mg/1)
Marketing started20180119
Package count6

External sources

Source: openFDA. Public-domain (CC0).