"67877-500-90" National Drug Code (NDC)

NDC Code	67877-500-90
Package Description	90 TABLET in 1 BOTTLE (67877-500-90)
Product NDC	67877-500
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Amlodipine And Olmesartan Medoxomil
Non-Proprietary Name	Amlodipine And Olmesartan Medoxomil
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20170814
Marketing Category Name	ANDA
Application Number	ANDA209042
Manufacturer	Ascend Laboratories, LLC
Substance Name	AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL
Strength	10; 20
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]