"33342-282-12" National Drug Code (NDC)

NDC Code	33342-282-12
Package Description	10 BLISTER PACK in 1 CARTON (33342-282-12) / 10 TABLET in 1 BLISTER PACK
Product NDC	33342-282
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	20241016
Marketing Category Name	ANDA
Application Number	ANDA207292
Manufacturer	Macleods Pharmaceuticals Limited
Substance Name	AMLODIPINE BESYLATE; VALSARTAN
Strength	10; 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]