Visitor Monitoring Drug Details: LEXAPRO
 
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Drug Details

Drug Name: LEXAPRO
FDA Application No: (NDA) 021323
Active Ingredient(s): ESCITALOPRAM OXALATE
Company: FOREST LABS
Original Approval or Tentative Approval Date: August 14, 2002
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
Therapeutic Equivalents Label Information
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
LEXAPRO ESCITALOPRAM OXALATEEQ 5MG BASETABLET; ORAL Prescription No AB
LEXAPRO ESCITALOPRAM OXALATEEQ 10MG BASETABLET; ORAL Prescription No AB
LEXAPRO ESCITALOPRAM OXALATEEQ 20MG BASETABLET; ORAL Prescription Yes AB


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