FDA NDC Directory · JSON-LD · Markdown

Amlodipine and Atorvastatin

NDC 71335-3076 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA205199
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAMLODIPINE BESYLATE (10 mg/1)
ATORVASTATIN CALCIUM TRIHYDRATE (10 mg/1)
Marketing started20200729
Package count1

External sources

Source: openFDA. Public-domain (CC0).