"72189-607-60" National Drug Code (NDC)

Lubiprostone 60 CAPSULE, GELATIN COATED in 1 BOTTLE (72189-607-60)
(Direct Rx)

NDC Code72189-607-60
Package Description60 CAPSULE, GELATIN COATED in 1 BOTTLE (72189-607-60)
Product NDC72189-607
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLubiprostone
Non-Proprietary NameLubiprostone
Dosage FormCAPSULE, GELATIN COATED
UsageORAL
Start Marketing Date20250116
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA021908
ManufacturerDirect Rx
Substance NameLUBIPROSTONE
Strength24
Strength Unitug/1
Pharmacy ClassesChloride Channel Activator [EPC], Chloride Channel Activators [MoA]

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