"0173-0556-02" National Drug Code (NDC)

NDC Code	0173-0556-02
Package Description	60 TABLET, FILM COATED in 1 BOTTLE (0173-0556-02)
Product NDC	0173-0556
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Zyban
Non-Proprietary Name	Bupropion Hydrochloride
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	19970528
Marketing Category Name	NDA
Application Number	NDA020711
Manufacturer	GlaxoSmithKline LLC
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]