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) 011790
Active Ingredient(s): METHOCARBAMOL
Company: BAXTER HLTHCARE CORP
 
Label History
 
View the label approved on May 4, 2004 for ROBAXIN, (NDA) 011790


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
5/4/2004 046Labeling Revision Letter
Label 
2/28/2001 042Control Supplement  
12/29/1999 041Manufacturing Change or Addition  
4/22/1998 040Manufacturing Change or Addition  
12/11/1990 038Package Change  
12/2/1988 037Control Supplement  
1/22/1987 036Control Supplement  
1/7/1987 035Control Supplement  
1/3/1986 034Manufacturing Change or Addition  
12/16/1982 033Manufacturing Change or Addition  
6/20/1983 032Labeling Revision  
9/3/1982 030Manufacturing Change or Addition  
9/29/1981 029Control Supplement  
1/22/1982 028Labeling Revision  
6/10/1981 027Labeling Revision  
1/3/1980 026Expiration Date Change  
5/23/1980 025Formulation Revision  
5/23/1980 024Manufacturing Change or Addition  
5/1/1980 023Manufacturing Change or Addition  
9/17/1979 022Manufacturing Change or Addition  
3/11/1976 012Control Supplement  
6/10/1959 000Approval  
 
Therapeutic Equivalents
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