Visitor Monitoring Drug History: MECLOFENAMATE SODIUM
 
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Label and Approval History

Drug Name: MECLOFENAMATE SODIUM
FDA Application No: (ANDA) 071080
Active Ingredient(s): MECLOFENAMATE SODIUM
Company: MYLAN
 
Label History
 
Labels are not available on this site for MECLOFENAMATE SODIUM, (ANDA) 071080
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/1/2002 013Control Supplement  
10/1/2002 012Expiration Date Change  
2/5/1998 011Chemistry  
5/5/1994 010Labeling  
1/28/1994 009Chemistry  
8/5/1992 007Labeling  
1/31/1990 006Chemistry  
8/4/1989 005Labeling  
2/8/1989 004Labeling  
4/9/1987 003Chemistry  
11/5/1986 002Chemistry  
9/3/1986 000Approval  
 
Therapeutic Equivalents
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