"70934-791-60" National Drug Code (NDC)

Bupropion Hydrochloride 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-791-60)
(Denton Pharma, Inc. dba Northwind Pharmaceuticals)

NDC Code70934-791-60
Package Description60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-791-60)
Product NDC70934-791
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name SuffixSr
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20200908
Marketing Category NameANDA
Application NumberANDA205794
ManufacturerDenton Pharma, Inc. dba Northwind Pharmaceuticals
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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