Visitor Monitoring Drug Details: ESTROPIPATE
 
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Drug Details

Drug Name: ESTROPIPATE
FDA Application No: (NDA) 040359
Active Ingredient(s): ESTROPIPATE
Company: MYLAN
Original Approval or Tentative Approval Date: August 26, 1999
 
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
ESTROPIPATE ESTROPIPATE0.75MGTABLET; ORAL Prescription No AB
ESTROPIPATE ESTROPIPATE1.5MGTABLET; ORAL Prescription No AB
ESTROPIPATE ESTROPIPATE3MGTABLET; ORAL Discontinued No None


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