"0024-5811-07" National Drug Code (NDC)

NDC Code	0024-5811-07
Package Description	7 TABLET, EXTENDED RELEASE in 1 BOTTLE (0024-5811-07)
Product NDC	0024-5811
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Aplenzin
Non-Proprietary Name	Bupropion Hydrobromide
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20090330
End Marketing Date	20170331
Marketing Category Name	NDA
Application Number	NDA022108
Manufacturer	sanofi-aventis U.S. LLC
Substance Name	BUPROPION HYDROBROMIDE
Strength	348
Strength Unit	mg/1
Pharmacy Classes	Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]