"69101-510-50" National Drug Code (NDC)

NDC Code	69101-510-50
Package Description	500 TABLET in 1 BOTTLE (69101-510-50)
Product NDC	69101-510
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Consensi
Non-Proprietary Name	Amlodipine Besylate And Celecoxib
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20191217
End Marketing Date	20221231
Marketing Category Name	NDA
Application Number	NDA210045
Manufacturer	Burke Therapeutics, LLC
Substance Name	AMLODIPINE BESYLATE; CELECOXIB
Strength	10; 200
Strength Unit	mg/1; mg/1
Pharmacy Classes	Anti-Inflammatory Agents, Non-Steroidal [CS], Calcium Channel Antagonists [MoA], Cyclooxygenase Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS], Nonsteroidal Anti-inflammatory Drug [EPC]