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"68788-7988-6" National Drug Code (NDC)

Bupropion Hydrochloride 60 TABLET, FILM COATED in 1 BOTTLE (68788-7988-6)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-7988-6
Package Description60 TABLET, FILM COATED in 1 BOTTLE (68788-7988-6)
Product NDC68788-7988
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210806
Marketing Category NameANDA
Application NumberANDA076143
ManufacturerPreferred Pharmaceuticals Inc.
Substance NameBUPROPION HYDROCHLORIDE
Strength100
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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