Visitor Monitoring Drug History: MECLOMEN
 
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: MECLOMEN
FDA Application No: (NDA) 018006
Active Ingredient(s): MECLOFENAMATE SODIUM
Company: PARKE DAVIS
 
Label History
 
Labels are not available on this site for MECLOMEN, (NDA) 018006
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/14/1990 019Manufacturing Change or Addition  
1/9/1989 018Labeling Revision  
6/7/1988 017Package Change  
12/10/1987 014Labeling Revision  
7/23/1990 013New or Modified Indication  
11/20/1985 012Labeling Revision  
7/23/1990 011New or Modified Indication  
5/15/1985 010Package Change  
8/30/1988 009New or Modified Indication  
4/9/1983 008Manufacturing Change or Addition  
2/13/1983 005Manufacturing Change or Addition  
5/10/1982 004Manufacturing Change or Addition  
11/22/1981 003Labeling Revision  
4/11/1981 002Control Supplement  
10/6/1980 001Formulation Revision  
6/25/1980 000Approval  
 
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