Visitor Monitoring Drug Details: ALORA
 
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Drug Details

Drug Name: ALORA
FDA Application No: (NDA) 020655
Active Ingredient(s): ESTRADIOL
Company: WATSON LABS
Original Approval or Tentative Approval Date: December 20, 1996
Chemical Type: 5 New manufacturer
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
ALORA ESTRADIOL0.05MG/24HRFILM, EXTENDED RELEASE; TRANSDERMAL Prescription No BX
ALORA ESTRADIOL0.075MG/24HRFILM, EXTENDED RELEASE; TRANSDERMAL Prescription No BX
ALORA ESTRADIOL0.1MG/24HRFILM, EXTENDED RELEASE; TRANSDERMAL Prescription No BX
ALORA ESTRADIOL0.025MG/24HRFILM, EXTENDED RELEASE; TRANSDERMAL Prescription No BX


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