Visitor Monitoring Drug Details: VIVELLE
 
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Drug Details

Drug Name: VIVELLE
FDA Application No: (NDA) 020323
Active Ingredient(s): ESTRADIOL
Company: NOVARTIS
Original Approval or Tentative Approval Date: October 28, 1994
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
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Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
VIVELLE ESTRADIOL0.0375MG/24HRFILM, EXTENDED RELEASE; TRANSDERMAL Discontinued No None
VIVELLE ESTRADIOL0.05MG/24HRFILM, EXTENDED RELEASE; TRANSDERMAL Prescription No AB1
VIVELLE ESTRADIOL0.075MG/24HRFILM, EXTENDED RELEASE; TRANSDERMAL Discontinued No None
VIVELLE ESTRADIOL0.1MG/24HRFILM, EXTENDED RELEASE; TRANSDERMAL Prescription No AB1
VIVELLE ESTRADIOL0.025MG/24HRFILM, EXTENDED RELEASE; TRANSDERMAL Discontinued No None


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