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"69339-162-17" National Drug Code (NDC)
Lubiprostone 40 BLISTER PACK in 1 CARTON (69339-162-17) / 1 CAPSULE in 1 BLISTER PACK (69339-162-98)
(Natco Pharma USA LLC)
NDC Code
69339-162-17
Package Description
40 BLISTER PACK in 1 CARTON (69339-162-17) / 1 CAPSULE in 1 BLISTER PACK (69339-162-98)
Product NDC
69339-162
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Lubiprostone
Non-Proprietary Name
Lubiprostone
Dosage Form
CAPSULE
Usage
ORAL
Start Marketing Date
20221017
Marketing Category Name
NDA AUTHORIZED GENERIC
Application Number
NDA021908
Manufacturer
Natco Pharma USA LLC
Substance Name
LUBIPROSTONE
Strength
8
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/69339-162-17