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Amlodipine and Atorvastatin

NDC 60505-3484 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerApotex Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA205199
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsAMLODIPINE BESYLATE (10 mg/1)
ATORVASTATIN CALCIUM TRIHYDRATE (20 mg/1)
Marketing started20200729
Package count1

External sources

Source: openFDA. Public-domain (CC0).