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) 085721
Active Ingredient(s): MEPROBAMATE
Company: WATSON LABS
 
Label History
 
Labels are not available on this site for MEPROBAMATE, (ANDA) 085721
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/20/1999 033Control Supplement  
1/21/1999 032Chemistry  
7/18/1997 031Chemistry  
7/18/1997 030Chemistry  
7/18/1997 029Chemistry  
4/22/1991 028Labeling  
2/2/1989 027Chemistry  
12/30/1988 026SBA  
2/2/1989 026Chemistry  
2/2/1989 025Chemistry  
4/14/1988 024Labeling  
12/24/1987 022Chemistry  
7/21/1987 021Chemistry  
7/21/1987 020Chemistry  
12/10/1986 018Chemistry  
1/18/1983 014Chemistry  
7/13/1977 000Approval  
 
Therapeutic Equivalents
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