Visitor Monitoring Drug History: ENOVID-E 21
 
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: ENOVID-E 21
FDA Application No: (NDA) 010976
Active Ingredient(s): MESTRANOL; NORETHYNODREL
Company: GD SEARLE LLC
 
Label History
 
Labels are not available on this site for ENOVIDE 21, (NDA) 010976
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/23/1986 073Labeling Revision  
6/10/1986 072Labeling Revision  
3/13/1986 071Labeling Revision  
6/5/1985 070Labeling Revision  
4/5/1985 069Labeling Revision  
9/18/1984 068Labeling Revision  
3/6/1984 066Labeling Revision  
6/3/1983 064Control Supplement  
6/23/1983 063Control Supplement  
11/22/1982 061Control Supplement  
2/22/1978 053Control Supplement  
2/12/1981 042Labeling Revision  
3/9/1961 000Approval  
 
There are no Therapeutic Equivalents
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