"68788-9255-9" National Drug Code (NDC)

NDC Code	68788-9255-9
Package Description	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9255-9)
Product NDC	68788-9255
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Bupropion
Non-Proprietary Name	Bupropion
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20141103
Marketing Category Name	ANDA
Application Number	ANDA201567
Manufacturer	Preferred Pharmaceuticals, Inc.
Substance Name	BUPROPION HYDROCHLORIDE
Strength	300
Strength Unit	mg/1
Pharmacy Classes	Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]