"66993-268-30" National Drug Code (NDC)

NDC Code	66993-268-30
Package Description	30 TABLET, COATED in 1 BOTTLE (66993-268-30)
Product NDC	66993-268
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Amlodipine And Atorvastatin
Non-Proprietary Name	Amlodipine And Atorvastatin
Dosage Form	TABLET, COATED
Usage	ORAL
Start Marketing Date	20220314
Marketing Category Name	NDA AUTHORIZED GENERIC
Application Number	NDA021540
Manufacturer	Prasco Laboratories
Substance Name	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE
Strength	5; 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]