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"72189-504-82" National Drug Code (NDC)
Baclofen 180 TABLET in 1 BOTTLE (72189-504-82)
(Direct_Rx)
NDC Code
72189-504-82
Package Description
180 TABLET in 1 BOTTLE (72189-504-82)
Product NDC
72189-504
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Baclofen
Non-Proprietary Name
Baclofen
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20230803
Marketing Category Name
ANDA
Application Number
ANDA209102
Manufacturer
Direct_Rx
Substance Name
BACLOFEN
Strength
20
Strength Unit
mg/1
Pharmacy Classes
GABA A Agonists [MoA], GABA B Agonists [MoA], gamma-Aminobutyric Acid-ergic Agonist [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72189-504-82