"21695-137-45" National Drug Code (NDC)

NDC Code	21695-137-45
Package Description	45 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-137-45)
Product NDC	21695-137
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Wellbutrin Xl
Non-Proprietary Name	Bupropion Hydrochloride
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20091223
Marketing Category Name	NDA
Application Number	NDA021515
Manufacturer	Rebel Distributors Corp
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]