"72162-2091-3" National Drug Code (NDC)

NDC Code	72162-2091-3
Package Description	30 TABLET, FILM COATED in 1 BOTTLE (72162-2091-3)
Product NDC	72162-2091
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Amlodipine And Atorvastatin
Non-Proprietary Name	Amlodipine And Atorvastatin
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20200729
Marketing Category Name	ANDA
Application Number	ANDA205199
Manufacturer	Bryant Ranch Prepack
Substance Name	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE
Strength	10; 40
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]