FDA NDC Directory · JSON-LD · Markdown

Atorvastatin calcium

NDC 60290-040 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerUmedica Laboratories USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA213853
Dosage form / routeTABLET · ORAL
Active ingredientsATORVASTATIN (20 mg/1)
Marketing started20260215
Package count4

External sources

Source: openFDA. Public-domain (CC0).