"70934-704-90" National Drug Code (NDC)

Bupropion Hydrochloride 90 TABLET in 1 BOTTLE, PLASTIC (70934-704-90)
(Denton Pharma, Inc. dba Northwind Pharmaceuticals)

NDC Code70934-704-90
Package Description90 TABLET in 1 BOTTLE, PLASTIC (70934-704-90)
Product NDC70934-704
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20200513
Marketing Category NameANDA
Application NumberANDA206975
ManufacturerDenton Pharma, Inc. dba Northwind Pharmaceuticals
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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