"69101-502-50" National Drug Code (NDC)

Consensi 500 TABLET in 1 BOTTLE (69101-502-50)
(Burke Therapeutics, LLC)

NDC Code69101-502-50
Package Description500 TABLET in 1 BOTTLE (69101-502-50)
Product NDC69101-502
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameConsensi
Non-Proprietary NameAmlodipine Besylate And Celecoxib
Dosage FormTABLET
UsageORAL
Start Marketing Date20191217
End Marketing Date20221231
Marketing Category NameNDA
Application NumberNDA210045
ManufacturerBurke Therapeutics, LLC
Substance NameAMLODIPINE BESYLATE; CELECOXIB
Strength2.5; 200
Strength Unitmg/1; mg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Calcium Channel Antagonists [MoA], Cyclooxygenase Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS], Nonsteroidal Anti-inflammatory Drug [EPC]

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