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Atorvastatin Calcium

NDC 42385-941 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLaurus Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA214513
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsATORVASTATIN CALCIUM TRIHYDRATE (20 mg/1)
Marketing started20240123
Package count6

External sources

Source: openFDA. Public-domain (CC0).