Visitor Monitoring Drug History: FEMHRT
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: FEMHRT
FDA Application No: (NDA) 021065
Active Ingredient(s): ETHINYL ESTRADIOL; NORETHINDRONE ACETATE
Company: WARNER CHILCOTT
 
Label History
 
View the label approved on January 21, 2005 for FEMHRT, (NDA) 021065


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/14/2005 012New Dosage Regimen Letter
Label 
1/20/2004 009Labeling Revision Letter
Label 
12/19/2000 006Control Supplement  
9/14/2000 005Manufacturing Change or Addition  
7/14/2000 004Labeling Revision  
4/20/2000 003Labeling Revision  
7/3/2000 002Manufacturing Change or Addition  
3/7/2000 001Manufacturing Change or Addition  
10/15/1999 000Approval Letter
Label
Review
Patient Package Insert 
 
There are no Therapeutic Equivalents
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