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"70710-1642-6" National Drug Code (NDC)
Lubiprostone 60 CAPSULE in 1 BOTTLE (70710-1642-6)
(Zydus Pharmaceuticals USA Inc.)
NDC Code
70710-1642-6
Package Description
60 CAPSULE in 1 BOTTLE (70710-1642-6)
Product NDC
70710-1642
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Lubiprostone
Non-Proprietary Name
Lubiprostone
Dosage Form
CAPSULE
Usage
ORAL
Start Marketing Date
20230323
Marketing Category Name
ANDA
Application Number
ANDA214131
Manufacturer
Zydus Pharmaceuticals USA Inc.
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/70710-1642-6