"0378-1722-93" National Drug Code (NDC)

NDC Code	0378-1722-93
Package Description	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-1722-93)
Product NDC	0378-1722
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	20150330
Marketing Category Name	ANDA
Application Number	ANDA090483
Manufacturer	Mylan Pharmaceuticals Inc.
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]