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"72189-429-20" National Drug Code (NDC)
Sucralfate 20 TABLET in 1 BOTTLE (72189-429-20)
(Direct_Rx)
NDC Code
72189-429-20
Package Description
20 TABLET in 1 BOTTLE (72189-429-20)
Product NDC
72189-429
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Sucralfate
Non-Proprietary Name
Sucralfate
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20230302
Marketing Category Name
ANDA
Application Number
ANDA074415
Manufacturer
Direct_Rx
Substance Name
SUCRALFATE
Strength
1
Strength Unit
g/1
Pharmacy Classes
Aluminum Complex [EPC], Organometallic Compounds [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72189-429-20