"63629-3762-1" National Drug Code (NDC)

NDC Code	63629-3762-1
Package Description	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-3762-1)
Product NDC	63629-3762
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Budeprion
Non-Proprietary Name	Bupropion Hydrochloride
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20080530
Marketing Category Name	ANDA
Application Number	ANDA077284
Manufacturer	Bryant Ranch Prepack
Substance Name	BUPROPION HYDROCHLORIDE
Strength	150
Strength Unit	mg/1
Pharmacy Classes	Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]