"10370-267-02" National Drug Code (NDC)

Lubiprostone 60 CAPSULE in 1 BOTTLE (10370-267-02)
(Par Pharmaceutical, Inc.)

NDC Code10370-267-02
Package Description60 CAPSULE in 1 BOTTLE (10370-267-02)
Product NDC10370-267
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLubiprostone
Non-Proprietary NameLubiprostone
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20200101
Marketing Category NameANDA
Application NumberANDA201442
ManufacturerPar Pharmaceutical, Inc.
Substance NameLUBIPROSTONE
Strength24
Strength Unitug/1
Pharmacy ClassesChloride Channel Activator [EPC], Chloride Channel Activators [MoA]

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