Visitor Monitoring Drug Details: VENLAFAXINE
 
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Drug Details

Drug Name: VENLAFAXINE
FDA Application No: (ANDA) 077166
Active Ingredient(s): VENLAFAXINE HYDROCHLORIDE
Company: MYLAN PHARMA
Original Approval or Tentative Approval Date: August 14, 2006
 
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
VENLAFAXINE VENLAFAXINE HYDROCHLORIDE25MGTABLET; ORAL Tentative Approval No None
VENLAFAXINE VENLAFAXINE HYDROCHLORIDE37.5MGTABLET; ORAL Tentative Approval No None
VENLAFAXINE VENLAFAXINE HYDROCHLORIDE50MGTABLET; ORAL Tentative Approval No None
VENLAFAXINE VENLAFAXINE HYDROCHLORIDE75MGTABLET; ORAL Tentative Approval No None
VENLAFAXINE VENLAFAXINE HYDROCHLORIDE100MGTABLET; ORAL Tentative Approval No None


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