"0781-1053-01" National Drug Code (NDC)

Bupropion Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (0781-1053-01)
(Sandoz Inc)

NDC Code0781-1053-01
Package Description100 TABLET, FILM COATED in 1 BOTTLE (0781-1053-01)
Product NDC0781-1053
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20000207
End Marketing Date20211130
Marketing Category NameANDA
Application NumberANDA075584
ManufacturerSandoz Inc
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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