"53217-358-90" National Drug Code (NDC)

Bupropion Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (53217-358-90)
(Aidarex Pharmaceuticals LLC)

NDC Code53217-358-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE (53217-358-90)
Product NDC53217-358
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20171226
Marketing Category NameANDA
Application NumberANDA076143
ManufacturerAidarex Pharmaceuticals LLC
Substance NameBUPROPION HYDROCHLORIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesAminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]

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