Visitor Monitoring Drug History: ROBAXIN
 
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: ROBAXIN
FDA Application No: (NDA) 011011
Active Ingredient(s): METHOCARBAMOL
Company: SCHWARZ PHARMA
 
Label History
 
View the label approved on May 6, 2003 for ROBAXIN, (NDA) 011011


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/1/2003 071Labeling Revision Letter
Label 
5/1/2003 070Labeling Revision Letter
Label 
4/22/1998 069Manufacturing Change or Addition  
8/21/1990 066Manufacturing Change or Addition  
1/6/1989 064Manufacturing Change or Addition  
1/28/1987 063Control Supplement  
4/16/1986 062Control Supplement  
4/16/1986 061Control Supplement  
10/25/1985 060Labeling Revision  
4/29/1985 059Manufacturing Change or Addition  
4/29/1985 058Manufacturing Change or Addition  
6/27/1984 057Control Supplement  
1/25/1983 055Control Supplement  
4/7/1983 054Package Change  
10/18/1982 053Control Supplement  
10/1/1982 052Control Supplement  
1/18/1982 050Control Supplement  
3/15/1982 049Expiration Date Change  
12/21/1981 048Manufacturing Change or Addition  
12/24/1981 047Control Supplement  
12/24/1981 046Control Supplement  
1/18/1982 044Control Supplement  
11/2/1981 043Control Supplement  
7/15/1982 042Package Change  
1/22/1981 041Formulation Revision  
1/22/1981 040Formulation Revision  
12/7/1981 039Labeling Revision  
10/28/1981 038Labeling Revision  
2/11/1980 032Manufacturing Change or Addition  
7/24/1979 031Manufacturing Change or Addition  
5/21/1979 022Manufacturing Change or Addition  
5/21/1979 020Labeling Revision  
5/21/1979 019Labeling Revision  
3/10/1976 018Control Supplement  
5/1/1975 017Control Supplement  
10/22/1974 015Labeling Revision  
4/29/1975 013Control Supplement  
4/29/1975 012Control Supplement  
12/9/1974 011Distributor  
10/17/1974 008Control Supplement  
7/16/1957 000Approval  
 
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