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"69680-158-92" National Drug Code (NDC)

Bupropion Hydrochloride (xl) 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-158-92)
(Vitruvias Therapeutics)

NDC Code69680-158-92
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-158-92)
Product NDC69680-158
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride (xl)
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20230417
Marketing Category NameANDA
Application NumberANDA208652
ManufacturerVitruvias Therapeutics
Substance NameBUPROPION HYDROCHLORIDE
Strength300
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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