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Pravastatin Sodium

NDC 35356-919 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namepravastatin sodium
Labeler / ManufacturerLake Erie Medical DBA Quality Care Products LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076341
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (20 mg/1)
Marketing started20110718
Marketing ended20280430
Package count2

External sources

Source: openFDA. Public-domain (CC0).