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PRAVASTATIN SODIUM

NDC 70518-0876 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA076341
Dosage form / routeTABLET · ORAL
Active ingredientsPRAVASTATIN SODIUM (40 mg/1)
Marketing started20171129
Package count1

External sources

Source: openFDA. Public-domain (CC0).