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Valsartan

NDC 65862-573 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202223
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVALSARTAN (320 mg/1)
Marketing started20150105
Package count2

External sources

Source: openFDA. Public-domain (CC0).