"66267-700-20" National Drug Code (NDC)

NDC Code	66267-700-20
Package Description	20 TABLET, FILM COATED in 1 BOTTLE (66267-700-20)
Product NDC	66267-700
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Bupropion Hydrochloride
Non-Proprietary Name	Bupropion Hydrochloride
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20060117
Marketing Category Name	ANDA
Application Number	ANDA076143
Manufacturer	NuCare Pharmaceuticals,Inc.
Substance Name	BUPROPION HYDROCHLORIDE
Strength	75
Strength Unit	mg/1
Pharmacy Classes	Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]