"0615-8526-39" National Drug Code (NDC)

NDC Code	0615-8526-39
Package Description	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8526-39)
Product NDC	0615-8526
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Bupropion
Non-Proprietary Name	Bupropion Hydrochloride
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20141101
End Marketing Date	20260131
Marketing Category Name	ANDA
Application Number	ANDA202304
Manufacturer	NCS HealthCare of KY, LLC dba Vangard Labs
Substance Name	BUPROPION HYDROCHLORIDE
Strength	100
Strength Unit	mg/1
Pharmacy Classes	Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA]