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"68788-7249-6" National Drug Code (NDC)

Bupropion 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7249-6)
(Preferred Pharmaceuticals Inc)

NDC Code68788-7249-6
Package Description60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7249-6)
Product NDC68788-7249
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20180827
Marketing Category NameANDA
Application NumberANDA202304
ManufacturerPreferred Pharmaceuticals Inc
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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