FDA NDC Directory · JSON-LD · Markdown

Amlodipine and atorvastatin

NDC 0378-4516 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMylan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA200465
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAMLODIPINE BESYLATE (5 mg/1)
ATORVASTATIN CALCIUM TRIHYDRATE (80 mg/1)
Marketing started20141010
Package count1

External sources

Source: openFDA. Public-domain (CC0).