FDA NDC Directory · JSON-LD · Markdown

Atorvastatin Calcium

NDC 42708-005 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerQPharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205300
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsATORVASTATIN CALCIUM TRIHYDRATE (40 mg/1)
Marketing started20170504
Package count1

External sources

Source: openFDA. Public-domain (CC0).