Visitor Monitoring Drug History: CLOMID
 
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: CLOMID
FDA Application No: (NDA) 016131
Active Ingredient(s): CLOMIPHENE CITRATE
Company: SANOFI AVENTIS US
 
Label History
 
Labels are not available on this site for CLOMID, (NDA) 016131
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/10/2002 025Control Supplement  
10/25/1995 024Labeling Revision  
9/30/1994 023Labeling Revision  
2/22/1994 022Manufacturing Change or Addition  
8/14/1991 021Control Supplement  
4/27/1988 019Package Change  
12/21/1993 017Labeling Revision  
11/18/1981 015Distributor  
6/23/1980 011Control Supplement  
6/23/1980 010Labeling Revision  
2/1/1967 000Approval  
 
Therapeutic Equivalents
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