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"50436-1580-1" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (50436-1580-1)
(Unit Dose Services)

NDC Code50436-1580-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE (50436-1580-1)
Product NDC50436-1580
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20060117
Marketing Category NameANDA
Application NumberANDA076143
ManufacturerUnit Dose Services
Substance NameBUPROPION HYDROCHLORIDE
Strength75
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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