Visitor Monitoring Drug Details: WELLBUTRIN SR
 
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Drug Details

Drug Name: WELLBUTRIN SR
FDA Application No: (NDA) 020358
Active Ingredient(s): BUPROPION HYDROCHLORIDE
Company: GLAXOSMITHKLINE
Original Approval or Tentative Approval Date: October 4, 1996
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
WELLBUTRIN SR BUPROPION HYDROCHLORIDE50MGTABLET, EXTENDED RELEASE; ORAL Prescription No None
WELLBUTRIN SR BUPROPION HYDROCHLORIDE100MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB1
WELLBUTRIN SR BUPROPION HYDROCHLORIDE150MGTABLET, EXTENDED RELEASE; ORAL Prescription Yes AB1
WELLBUTRIN SR BUPROPION HYDROCHLORIDE200MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB1


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