"70771-1764-1" National Drug Code (NDC)

Lubiprostone 100 CAPSULE in 1 BOTTLE (70771-1764-1)
(Zydus Lifesciences Limited)

NDC Code70771-1764-1
Package Description100 CAPSULE in 1 BOTTLE (70771-1764-1)
Product NDC70771-1764
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLubiprostone
Non-Proprietary NameLubiprostone
Dosage FormCAPSULE
UsageORAL
Start Marketing Date20230323
Marketing Category NameANDA
Application NumberANDA214131
ManufacturerZydus Lifesciences Limited
Substance NameLUBIPROSTONE
Strength24
Strength Unitug/1
Pharmacy ClassesChloride Channel Activator [EPC], Chloride Channel Activators [MoA]

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