"68180-766-06" National Drug Code (NDC)

NDC Code	68180-766-06
Package Description	30 TABLET in 1 BOTTLE (68180-766-06)
Product NDC	68180-766
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Amlodipine And Valsartan
Non-Proprietary Name	Amlodipine And Valsartan
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20150331
Marketing Category Name	ANDA
Application Number	ANDA090245
Manufacturer	Lupin Pharmaceuticals, Inc.
Substance Name	AMLODIPINE BESYLATE; VALSARTAN
Strength	5; 320
Strength Unit	mg/1; mg/1
Pharmacy Classes	Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]