Visitor Monitoring Drug Details: BUPROPION HYDROCHLORIDE
 
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Drug Details

Drug Name: BUPROPION HYDROCHLORIDE
FDA Application No: (ANDA) 075584
Active Ingredient(s): BUPROPION HYDROCHLORIDE
Company: SANDOZ
Original Approval or Tentative Approval Date: February 7, 2000
 
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 HYDROCHLORIDE75MGTABLET; ORAL Prescription No AB
BUPROPION HYDROCHLORIDE BUPROPION HYDROCHLORIDE100MGTABLET; ORAL Prescription No AB


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