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"68788-6809-3" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-6809-3)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-6809-3
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-6809-3)
Product NDC68788-6809
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name Suffix(xl)
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20161107
Marketing Category NameANDA
Application NumberANDA206556
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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