Visitor Monitoring Drug Details: FEMRING
 
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Drug Details

Drug Name: FEMRING
FDA Application No: (NDA) 021367
Active Ingredient(s): ESTRADIOL ACETATE
Company: GALEN LTD
Original Approval or Tentative Approval Date: March 20, 2003
Chemical Type: 2 New active ingredient
Review Classification: S Standard review drug
 
 
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
FEMRING ESTRADIOL ACETATEEQ 0.05MG BASE/24HRINSERT, EXTENDED RELEASE; VAGINAL Prescription No None
FEMRING ESTRADIOL ACETATEEQ 0.1MG BASE/24HRINSERT, EXTENDED RELEASE; VAGINAL Prescription Yes None


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