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"72189-457-30" National Drug Code (NDC)
Bupropion Hcl 30 TABLET, FILM COATED in 1 BOTTLE (72189-457-30)
(Direct_Rx)
NDC Code
72189-457-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (72189-457-30)
Product NDC
72189-457
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion Hcl
Non-Proprietary Name
Bupropion Hcl
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20230330
Marketing Category Name
ANDA
Application Number
ANDA076143
Manufacturer
Direct_Rx
Substance Name
BUPROPION HYDROCHLORIDE
Strength
100
Strength Unit
mg/1
Pharmacy Classes
Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72189-457-30