Visitor Monitoring Drug Details: ESCITALOPRAM OXALATE
 
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Drug Details

Drug Name: ESCITALOPRAM OXALATE
FDA Application No: (ANDA) 077798
Active Ingredient(s): ESCITALOPRAM OXALATE
Company: DR REDDYS LABS INC
Original Approval or Tentative Approval Date: July 16, 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 OXALATE5MGTABLET; ORAL Tentative Approval No None
ESCITALOPRAM OXALATE ESCITALOPRAM OXALATE10MGTABLET; ORAL Tentative Approval No None
ESCITALOPRAM OXALATE ESCITALOPRAM OXALATE20MGTABLET; ORAL Tentative Approval No None


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