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"43602-549-30" National Drug Code (NDC)
Lubiprostone 30 CAPSULE in 1 BOTTLE (43602-549-30)
(Ascent Pharmaceuticals, Inc.)
NDC Code
43602-549-30
Package Description
30 CAPSULE in 1 BOTTLE (43602-549-30)
Product NDC
43602-549
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Lubiprostone
Non-Proprietary Name
Lubiprostone
Dosage Form
CAPSULE
Usage
ORAL
Start Marketing Date
20250102
Marketing Category Name
ANDA
Application Number
ANDA218640
Manufacturer
Ascent Pharmaceuticals, Inc.
Substance Name
LUBIPROSTONE
Strength
.024
Strength Unit
mg/1
Pharmacy Classes
Chloride Channel Activator [EPC], Chloride Channel Activators [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/43602-549-30