"71205-832-55" National Drug Code (NDC)

Lubiprostone 500 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-55)
(Proficient Rx LP)

NDC Code71205-832-55
Package Description500 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-55)
Product NDC71205-832
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLubiprostone
Non-Proprietary NameLubiprostone
Dosage FormCAPSULE, GELATIN COATED
UsageORAL
Start Marketing Date20230101
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA021908
ManufacturerProficient Rx LP
Substance NameLUBIPROSTONE
Strength24
Strength Unitug/1
Pharmacy ClassesChloride Channel Activator [EPC], Chloride Channel Activators [MoA]

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