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"68682-581-30" National Drug Code (NDC)

Bupropion Hydrobromide 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-581-30)
(Oceanside Pharmaceuticals)

NDC Code68682-581-30
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-581-30)
Product NDC68682-581
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrobromide
Non-Proprietary NameBupropion Hydrobromide
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20260629
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA022108
ManufacturerOceanside Pharmaceuticals
Substance NameBUPROPION HYDROBROMIDE
Strength348
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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