"64455-731-30" National Drug Code (NDC)

NDC Code	64455-731-30
Package Description	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (64455-731-30)
Product NDC	64455-731
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Wellbutrin
Proprietary Name Suffix	Xl
Non-Proprietary Name	Bupropion Hydrochloride
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20091223
End Marketing Date	20140430
Marketing Category Name	NDA
Application Number	NDA021515
Manufacturer	BTA Pharmaceuticals
Substance Name	BUPROPION HYDROCHLORIDE
Strength	300
Strength Unit	mg/1
Pharmacy Classes	Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]