Visitor Monitoring Drug Details: BUPROPION HYDROCHLORIDE
 
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Drug Details

Drug Name: BUPROPION HYDROCHLORIDE
FDA Application No: (ANDA) 077715
Active Ingredient(s): BUPROPION HYDROCHLORIDE
Company: WATSON LABS
Original Approval or Tentative Approval Date: June 13, 2007
 
Therapeutic Equivalents Labels are not available
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
BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE150MGTABLET, EXTENDED RELEASE; ORAL Tentative Approval No None
BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE300MGTABLET, EXTENDED RELEASE; ORAL Prescription No AB3


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