Visitor Monitoring Drug History: MECLOFENAMATE SODIUM
 
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Label and Approval History

Drug Name: MECLOFENAMATE SODIUM
FDA Application No: (ANDA) 071468
Active Ingredient(s): MECLOFENAMATE SODIUM
Company: WATSON LABS
 
Label History
 
Labels are not available on this site for MECLOFENAMATE SODIUM, (ANDA) 071468
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/25/2001 021Control Supplement  
6/29/1998 019Chemistry  
10/21/1994 018Labeling  
4/29/1996 017Chemistry  
6/25/1992 016Chemistry  
1/28/1991 015Chemistry  
8/7/1991 014Chemistry  
6/29/1990 013Chemistry  
2/19/1993 013Labeling  
4/17/1989 012Labeling  
2/14/1989 011Labeling  
8/29/1988 010Labeling  
7/12/1988 009Chemistry  
7/12/1988 008Chemistry  
7/12/1988 007Chemistry  
11/6/1987 002Chemistry  
11/6/1987 001Chemistry  
4/15/1987 000Approval  
 
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