"67767-141-30" National Drug Code (NDC)

NDC Code	67767-141-30
Package Description	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (67767-141-30)
Product NDC	67767-141
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	20100331
End Marketing Date	20160131
Marketing Category Name	ANDA
Application Number	ANDA077285
Manufacturer	Actavis South Atlantic 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]