"0185-1111-52" National Drug Code (NDC)

NDC Code	0185-1111-52
Package Description	250 TABLET, EXTENDED RELEASE in 1 BOTTLE (0185-1111-52)
Product NDC	0185-1111
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Bupropion Hydrochloride
Non-Proprietary Name	Bupropion Hydrochloride
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20050622
Marketing Category Name	ANDA
Application Number	ANDA075932
Manufacturer	Eon Labs, Inc.
Substance Name	BUPROPION HYDROCHLORIDE
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA]