"0093-5351-56" National Drug Code (NDC)

NDC Code	0093-5351-56
Package Description	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0093-5351-56)
Product NDC	0093-5351
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Budeprion
Proprietary Name Suffix	Xl
Non-Proprietary Name	Bupropion Hydrochloride
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20061215
End Marketing Date	20140630
Marketing Category Name	ANDA
Application Number	ANDA077415
Manufacturer	TEVA Pharmaceuticals USA 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]