"65862-739-03" National Drug Code (NDC)

NDC Code	65862-739-03
Package Description	3 BLISTER PACK in 1 CARTON (65862-739-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-739-10)
Product NDC	65862-739
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Amlodipine And Valsartan
Non-Proprietary Name	Amlodipine And Valsartan
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20160422
Marketing Category Name	ANDA
Application Number	ANDA206512
Manufacturer	Aurobindo Pharma Limited
Substance Name	AMLODIPINE BESYLATE; VALSARTAN
Strength	10; 160
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]