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"71205-832-55" National Drug Code (NDC)
Lubiprostone 500 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-55)
(Proficient Rx LP)
NDC Code
71205-832-55
Package Description
500 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-832-55)
Product NDC
71205-832
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Lubiprostone
Non-Proprietary Name
Lubiprostone
Dosage Form
CAPSULE, GELATIN COATED
Usage
ORAL
Start Marketing Date
20230101
Marketing Category Name
NDA AUTHORIZED GENERIC
Application Number
NDA021908
Manufacturer
Proficient Rx LP
Substance Name
LUBIPROSTONE
Strength
24
Strength Unit
ug/1
Pharmacy Classes
Chloride Channel Activator [EPC], Chloride Channel Activators [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71205-832-55