"23155-844-03" National Drug Code (NDC)

NDC Code	23155-844-03
Package Description	30 TABLET in 1 BOTTLE, PLASTIC (23155-844-03)
Product NDC	23155-844
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	20230315
Marketing Category Name	ANDA
Application Number	ANDA090011
Manufacturer	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Substance Name	AMLODIPINE; VALSARTAN
Strength	5; 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]