Visitor Monitoring Drug Details: WELLBUTRIN XL
 
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Drug Details

Drug Name: WELLBUTRIN XL
FDA Application No: (NDA) 021515
Active Ingredient(s): BUPROPION HYDROCHLORIDE
Company: SMITHKLINE BEECHAM
Original Approval or Tentative Approval Date: August 29, 2003
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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 XL BUPROPION HYDROCHLORIDE150MGTABLET, EXTENDED RELEASE; ORAL Prescription Yes AB3
WELLBUTRIN XL BUPROPION HYDROCHLORIDE300MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB3


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