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"68788-7283-2" National Drug Code (NDC)

Bupropion 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7283-2)
(Preferred Pharmaceuticals, Inc.)

NDC Code68788-7283-2
Package Description20 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7283-2)
Product NDC68788-7283
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20141101
Marketing Category NameANDA
Application NumberANDA202304
ManufacturerPreferred Pharmaceuticals, Inc.
Substance NameBUPROPION HYDROCHLORIDE
Strength200
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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