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"53217-358-90" National Drug Code (NDC)
Bupropion Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (53217-358-90)
(Aidarex Pharmaceuticals LLC)
NDC Code
53217-358-90
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (53217-358-90)
Product NDC
53217-358
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion Hydrochloride
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20171226
Marketing Category Name
ANDA
Application Number
ANDA076143
Manufacturer
Aidarex Pharmaceuticals LLC
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/53217-358-90