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atorvastatin calcium

NDC 70710-1770 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA206536
Dosage form / routeTABLET · ORAL
Active ingredientsATORVASTATIN CALCIUM TRIHYDRATE (80 mg/1)
Marketing started20240612
Package count3

External sources

Source: openFDA. Public-domain (CC0).