"0093-5501-01" National Drug Code (NDC)

NDC Code	0093-5501-01
Package Description	100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0093-5501-01)
Product NDC	0093-5501
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Budeprion
Proprietary Name Suffix	Sr
Non-Proprietary Name	Bupropion Hydrochloride
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20040219
End Marketing Date	20141031
Marketing Category Name	ANDA
Application Number	ANDA075913
Manufacturer	TEVA Pharmaceuticals USA Inc
Substance Name	BUPROPION HYDROCHLORIDE
Strength	100
Strength Unit	mg/1
Pharmacy Classes	Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]