"68788-9669-3" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-9669-3)
(Preferred Pharmaceuticals, Inc.)

NDC Code68788-9669-3
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-9669-3)
Product NDC68788-9669
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20130725
Marketing Category NameANDA
Application NumberANDA078866
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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