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Atorvastatin calcium

NDC 82804-056 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA213853
Dosage form / routeTABLET · ORAL
Active ingredientsATORVASTATIN (40 mg/1)
Marketing started20200826
Package count3

External sources

Source: openFDA. Public-domain (CC0).