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"60687-827-32" National Drug Code (NDC)
Lubiprostone 20 BLISTER PACK in 1 CARTON (60687-827-32) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK (60687-827-33)
(American Health Packaging)
NDC Code
60687-827-32
Package Description
20 BLISTER PACK in 1 CARTON (60687-827-32) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK (60687-827-33)
Product NDC
60687-827
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Lubiprostone
Non-Proprietary Name
Lubiprostone
Dosage Form
CAPSULE, GELATIN COATED
Usage
ORAL
Start Marketing Date
20251126
Marketing Category Name
ANDA
Application Number
ANDA209920
Manufacturer
American Health Packaging
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/60687-827-32