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ATORVASTATIN CALCIUM

NDC 50228-452 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerScieGen Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205519
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsATORVASTATIN CALCIUM TRIHYDRATE (20 mg/1)
Marketing started20160519
Package count2

External sources

Source: openFDA. Public-domain (CC0).