"51079-944-20" National Drug Code (NDC)

NDC Code	51079-944-20
Package Description	100 BLISTER PACK in 1 CARTON (51079-944-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-944-01)
Product NDC	51079-944
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Bupropion Hydrochloride
Non-Proprietary Name	Bupropion Hydrochloride
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20000701
End Marketing Date	20200930
Marketing Category Name	ANDA
Application Number	ANDA075491
Manufacturer	Mylan Institutional Inc.
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]