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"63304-352-60" National Drug Code (NDC)

Lubiprostone 60 CAPSULE, GELATIN COATED in 1 BOTTLE (63304-352-60)
(Sun Pharmaceutical Industries, Inc.)

NDC Code63304-352-60
Package Description60 CAPSULE, GELATIN COATED in 1 BOTTLE (63304-352-60)
Product NDC63304-352
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLubiprostone
Non-Proprietary NameLubiprostone
Dosage FormCAPSULE, GELATIN COATED
UsageORAL
Start Marketing Date20230101
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA021908
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameLUBIPROSTONE
Strength24
Strength Unitug/1
Pharmacy ClassesChloride Channel Activator [EPC], Chloride Channel Activators [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/63304-352-60





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