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ATORVASTATIN CALCIUM

NDC 70518-1322 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA090548
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE (40 mg/1)
Marketing started20180725
Package count3

External sources

Source: openFDA. Public-domain (CC0).