"71765-002-50" National Drug Code (NDC)

NDC Code	71765-002-50
Package Description	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (71765-002-50)
Product NDC	71765-002
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Bupropion Hydrochloride
Proprietary Name Suffix	Xl
Non-Proprietary Name	Bupropion Hydrochloride
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20201206
Marketing Category Name	ANDA
Application Number	ANDA211200
Manufacturer	Zhejiang Jutai Pharamceutical Co., Ltd
Substance Name	BUPROPION HYDROCHLORIDE
Strength	300
Strength Unit	mg/1
Pharmacy Classes	Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]