"68071-2586-9" National Drug Code (NDC)

NDC Code	68071-2586-9
Package Description	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-2586-9)
Product NDC	68071-2586
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	20181108
Marketing Category Name	ANDA
Application Number	ANDA210497
Manufacturer	NuCare Pharmaceuticals,Inc.
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]