"70934-985-90" National Drug Code (NDC)

Bupropion Hydrochloride 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-985-90)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-985-90
Package Description90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-985-90)
Product NDC70934-985
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name SuffixSr
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20220701
End Marketing Date20231130
Marketing Category NameANDA
Application NumberANDA211347
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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