"43602-549-05" National Drug Code (NDC)

Lubiprostone 500 CAPSULE in 1 BOTTLE (43602-549-05)
(Ascent Pharmaceuticals, Inc.)

NDC Code43602-549-05
Package Description500 CAPSULE in 1 BOTTLE (43602-549-05)
Product NDC43602-549
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLubiprostone
Non-Proprietary NameLubiprostone
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20250102
Marketing Category NameANDA
Application NumberANDA218640
ManufacturerAscent Pharmaceuticals, Inc.
Substance NameLUBIPROSTONE
Strength.024
Strength Unitmg/1
Pharmacy ClassesChloride Channel Activator [EPC], Chloride Channel Activators [MoA]

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