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

Drug Name: EFFEXOR
FDA Application No: (NDA) 020151
Active Ingredient(s): VENLAFAXINE HYDROCHLORIDE
Company: WYETH PHARMS INC
Original Approval or Tentative Approval Date: December 28, 1993
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
EFFEXOR VENLAFAXINE HYDROCHLORIDEEQ 12.5MG BASETABLET; ORAL Discontinued No None
EFFEXOR VENLAFAXINE HYDROCHLORIDEEQ 25MG BASETABLET; ORAL Prescription No AB
EFFEXOR VENLAFAXINE HYDROCHLORIDEEQ 50MG BASETABLET; ORAL Prescription Yes AB
EFFEXOR VENLAFAXINE HYDROCHLORIDEEQ 75MG BASETABLET; ORAL Prescription No AB
EFFEXOR VENLAFAXINE HYDROCHLORIDEEQ 100MG BASETABLET; ORAL Prescription No AB
EFFEXOR VENLAFAXINE HYDROCHLORIDEEQ 37.5MG BASETABLET; ORAL Prescription No AB


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