"76519-1021-3" National Drug Code (NDC)

NDC Code	76519-1021-3
Package Description	30 TABLET, EXTENDED RELEASE in 1 CONTAINER (76519-1021-3)
Product NDC	76519-1021
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	20170103
Marketing Category Name	ANDA
Application Number	ANDA206556
Manufacturer	H.J. Harkins Company 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]