WELLBUTRIN - 0173-0135-55 - (bupropion hydrochloride)

Alphabetical Index


Drug Information of WELLBUTRIN

Product NDC: 0173-0135
Proprietary Name: WELLBUTRIN
Non Proprietary Name: bupropion hydrochloride
Active Ingredient(s): 150    mg/1 & nbsp;   bupropion hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of WELLBUTRIN

Product NDC: 0173-0135
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020358
Marketing Category: NDA
Start Marketing Date: 19961115

Package Information of WELLBUTRIN

Package NDC: 0173-0135-55
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (0173-0135-55)

NDC Information of WELLBUTRIN

NDC Code 0173-0135-55
Proprietary Name WELLBUTRIN
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (0173-0135-55)
Product NDC 0173-0135
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name bupropion hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19961115
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name BUPROPION HYDROCHLORIDE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]

Complete Information of WELLBUTRIN


General Information