Visitor Monitoring Drug History: SOMA
 
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: SOMA
FDA Application No: (NDA) 011792
Active Ingredient(s): CARISOPRODOL
Company: MEDPOINTE PHARM HLC
 
Label History
 
View the label approved on September 19, 2007 for SOMA, (NDA) 011792


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
9/13/2007 041New Dosage Regimen Letter
Label 
12/29/1999 036Package Change  
6/8/2006 035Labeling Revision Letter
Label 
10/25/1993 032Control Supplement  
3/2/1994 031Control Supplement  
11/10/1987 030Package Change  
9/1/1987 029Control Supplement  
10/27/1986 028Labeling Revision  
4/30/1986 027Package Change  
11/27/1987 026Formulation Revision  
4/19/1983 025Control Supplement  
3/18/1983 024Control Supplement  
3/18/1983 023Manufacturing Change or Addition  
10/27/1981 021Manufacturing Change or Addition  
4/13/1979 020Manufacturing Change or Addition  
11/30/1979 019Control Supplement  
12/5/1979 018Formulation Revision  
5/20/1975 017Labeling Revision  
11/8/1974 016Distributor  
7/19/1974 015Distributor  
12/13/1974 014Control Supplement  
4/9/1959 000Approval  
 
Therapeutic Equivalents
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