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"68788-7121-1" National Drug Code (NDC)

Bupropion Hydrochloride 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7121-1)
(Preferred Pharmaceuticals, Inc.)

NDC Code68788-7121-1
Package Description100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7121-1)
Product NDC68788-7121
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20180322
Marketing Category NameANDA
Application NumberANDA090693
ManufacturerPreferred Pharmaceuticals, Inc.
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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