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"70771-1764-1" National Drug Code (NDC)
Lubiprostone 100 CAPSULE in 1 BOTTLE (70771-1764-1)
(Zydus Lifesciences Limited)
NDC Code
70771-1764-1
Package Description
100 CAPSULE in 1 BOTTLE (70771-1764-1)
Product NDC
70771-1764
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 Lifesciences Limited
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/70771-1764-1