"58151-067-93" National Drug Code (NDC)

NDC Code	58151-067-93
Package Description	30 TABLET, FILM COATED in 1 BOTTLE (58151-067-93)
Product NDC	58151-067
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Caduet
Non-Proprietary Name	Amlodipine And Atorvastatin
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20260226
Marketing Category Name	NDA
Application Number	NDA021540
Manufacturer	Viatris Specialty LLC
Substance Name	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE
Strength	5; 80
Strength Unit	mg/1; mg/1
Pharmacy Classes	Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS], HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]