Visitor Monitoring Drug Details: ESCITALOPRAM OXALATE
 
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Drug Details

Drug Name: ESCITALOPRAM OXALATE
FDA Application No: (ANDA) 076765
Active Ingredient(s): ESCITALOPRAM OXALATE
Company: IVAX PHARMS
Original Approval or Tentative Approval Date: February 6, 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
ESCITALOPRAM OXALATE ESCITALOPRAM OXALATEEQ 5MG BASETABLET; ORAL Prescription No AB
ESCITALOPRAM OXALATE ESCITALOPRAM OXALATEEQ 10MG BASETABLET; ORAL Prescription No AB
ESCITALOPRAM OXALATE ESCITALOPRAM OXALATEEQ 20MG BASETABLET; ORAL Prescription No AB


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