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) 018052
Active Ingredient(s): CLOTRIMAZOLE
Company: SCHERING PLOUGH
 
Label History
 
Labels are not available on this site for GYNELOTRIMIN, (NDA) 018052
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/16/2002 030Control Supplement  
2/2/2001 029Control Supplement  
9/1/2000 028Control Supplement  
1/20/2000 027Manufacturing Change or Addition  
12/9/1998 026Package Change  
8/11/1998 025Package Change  
4/26/1993 024New or Modified Indication  
4/15/1993 023Package Change  
10/8/1992 022Labeling Revision  
4/21/1993 021Package Change  
5/12/1992 020Labeling Revision  
4/14/1992 019Labeling Revision  
9/22/1993 018Manufacturing Change or Addition  
6/23/1992 017Control Supplement  
9/11/1990 014Control Supplement  
10/4/1988 013Control Supplement  
11/30/1990 012OTC Labeling  
6/18/1987 011Control Supplement  
9/12/1986 010Manufacturing Change or Addition  
5/20/1986 009Control Supplement  
7/24/1985 007Package Change  
8/17/1981 006Control Supplement  
10/9/1981 005Control Supplement  
12/4/1986 004Practioner Draft Labeling  
3/27/1981 003Control Supplement  
1/3/1980 002Package Change  
11/27/1979 001Distributor  
11/8/1978 000Approval  
 
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