"43602-548-30" National Drug Code (NDC)

Lubiprostone 30 CAPSULE in 1 BOTTLE (43602-548-30)
(Ascent Pharmaceuticals, Inc.)

NDC Code43602-548-30
Package Description30 CAPSULE in 1 BOTTLE (43602-548-30)
Product NDC43602-548
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.008
Strength Unitmg/1
Pharmacy ClassesChloride Channel Activator [EPC], Chloride Channel Activators [MoA]

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