Visitor Monitoring Drug Details: ZYBAN
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Drug Details

Drug Name: ZYBAN
FDA Application No: (NDA) 020711
Active Ingredient(s): BUPROPION HYDROCHLORIDE
Company: GLAXOSMITHKLINE
Original Approval or Tentative Approval Date: May 14, 1997
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
ZYBAN BUPROPION HYDROCHLORIDE100MGTABLET, EXTENDED RELEASE; ORAL Discontinued No None
ZYBAN BUPROPION HYDROCHLORIDE150MGTABLET, EXTENDED RELEASE; ORAL Prescription Yes AB2


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