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"68788-6808-2" National Drug Code (NDC)

Bupropion Hydrochloride 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-6808-2)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-6808-2
Package Description20 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-6808-2)
Product NDC68788-6808
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20161107
Marketing Category NameANDA
Application NumberANDA075932
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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