"60505-3492-3" National Drug Code (NDC)

NDC Code	60505-3492-3
Package Description	30 TABLET, FILM COATED in 1 BOTTLE (60505-3492-3)
Product NDC	60505-3492
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	Apotex Corp.
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]