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Atorvastatin Calcium

NDC 76420-945 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAsclemed USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209288
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsATORVASTATIN CALCIUM TRIHYDRATE (20 mg/1)
Marketing started20181223
Package count9

External sources

Source: openFDA. Public-domain (CC0).