Visitor Monitoring Drug History: GYNE-LOTRIMIN
 
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: GYNE-LOTRIMIN
FDA Application No: (NDA) 017717
Active Ingredient(s): CLOTRIMAZOLE
Company: SCHERING PLOUGH
 
Label History
 
Labels are not available on this site for GYNELOTRIMIN, (NDA) 017717
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/3/1999 025Control Supplement  
3/17/1998 023Manufacturing Change or Addition  
2/27/1997 022Package Change  
10/8/1992 021Labeling Revision  
4/14/1992 020Labeling Revision  
6/23/1992 019Control Supplement  
11/30/1990 016OTC Labeling  
6/18/1987 014Control Supplement  
5/20/1986 013Control Supplement  
9/16/1982 012Labeling Revision  
11/12/1981 011Labeling Revision  
8/5/1981 008Control Supplement  
12/11/1980 007Expiration Date Change  
9/23/1980 006Labeling Revision  
7/16/1979 005Package Change  
7/23/1979 004Manufacturing Change or Addition  
5/18/1978 003Manufacturing Change or Addition  
9/15/1977 002Manufacturing Change or Addition  
8/9/1977 001Manufacturing Change or Addition  
3/24/1976 000Approval  
 
Therapeutic Equivalents
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