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Valsartan

NDC 42385-992 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLaurus Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA218897
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVALSARTAN (320 mg/1)
Marketing started20260422
Package count4

External sources

Source: openFDA. Public-domain (CC0).