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"70771-1763-1" National Drug Code (NDC)
Lubiprostone 100 CAPSULE in 1 BOTTLE (70771-1763-1)
(Zydus Lifesciences Limited)
NDC Code
70771-1763-1
Package Description
100 CAPSULE in 1 BOTTLE (70771-1763-1)
Product NDC
70771-1763
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
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/70771-1763-1