"31722-404-60" National Drug Code (NDC)

Lubiprostone 60 CAPSULE in 1 BOTTLE (31722-404-60)
(Camber Pharmaceuticals, Inc.)

NDC Code31722-404-60
Package Description60 CAPSULE in 1 BOTTLE (31722-404-60)
Product NDC31722-404
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLubiprostone
Non-Proprietary NameLubiprostone
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20250527
Marketing Category NameANDA
Application NumberANDA218640
ManufacturerCamber Pharmaceuticals, Inc.
Substance NameLUBIPROSTONE
Strength.024
Strength Unitmg/1
Pharmacy ClassesChloride Channel Activator [EPC], Chloride Channel Activators [MoA]

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