Visitor Monitoring Drug History: MEPROBAMATE
 
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: MEPROBAMATE
FDA Application No: (ANDA) 085720
Active Ingredient(s): MEPROBAMATE
Company: WATSON LABS
 
Label History
 
Labels are not available on this site for MEPROBAMATE, (ANDA) 085720
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/20/1999 031Control Supplement  
1/21/1999 030Chemistry  
7/18/1997 029Chemistry  
7/18/1997 028Chemistry  
3/26/1997 027Chemistry  
11/10/1988 026SBA  
4/22/1991 026Labeling  
3/28/1988 022Labeling  
12/24/1987 020Chemistry  
7/21/1987 019Chemistry  
7/21/1987 018Chemistry  
12/10/1986 016Chemistry  
12/7/1981 007Chemistry  
7/13/1977 000Approval  
 
Therapeutic Equivalents
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