"0093-5703-01" National Drug Code (NDC)

Buproban 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0093-5703-01)
(TEVA Pharmaceuticals USA Inc)

NDC Code0093-5703-01
Package Description100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0093-5703-01)
Product NDC0093-5703
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBuproban
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20040527
Marketing Category NameANDA
Application NumberANDA075914
ManufacturerTEVA Pharmaceuticals USA Inc
Substance NameBUPROPION HYDROCHLORIDE
Strength150
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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