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Pravastatin sodium

NDC 65862-633 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA203367
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (20 mg/1)
Marketing started20170202
Package count3

External sources

Source: openFDA. Public-domain (CC0).