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
 
 
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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