Visitor Monitoring Drug History: DANTRIUM
 
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: DANTRIUM
FDA Application No: (NDA) 017443
Active Ingredient(s): DANTROLENE SODIUM
Company: PROCTER AND GAMBLE
 
Label History
 
Labels are not available on this site for DANTRIUM, (NDA) 017443
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/30/1997 047Control Supplement  
3/14/1997 045Control Supplement  
9/18/1996 044Manufacturing Change or Addition  
1/24/1992 041Package Change  
5/20/1991 040Control Supplement  
2/14/1990 039Package Change  
6/29/1989 038Package Change  
7/23/1985 036Labeling Revision  
5/20/1985 035Control Supplement  
5/16/1983 033Control Supplement  
5/16/1983 032Control Supplement  
5/16/1983 031Control Supplement  
5/16/1983 030Control Supplement  
5/16/1983 029Control Supplement  
11/18/1983 028Manufacturing Change or Addition  
9/29/1982 025Labeling Revision  
10/9/1981 024Labeling Revision  
3/18/1981 023Formulation Revision  
9/17/1979 022Package Change  
8/15/1979 021Package Change  
8/15/1979 020Package Change  
7/5/1979 019Manufacturing Change or Addition  
6/27/1977 017Formulation Revision  
10/25/1977 016Labeling Revision  
6/15/1977 015Labeling Revision  
6/15/1977 013Formulation Revision  
5/12/1976 012Expiration Date Change  
7/16/1976 011Manufacturing Change or Addition  
5/12/1976 010Package Change  
10/10/1975 009Labeling Revision  
7/15/1975 008Labeling Revision  
11/20/1975 007Control Supplement  
11/19/1975 006Labeling Revision  
2/26/1975 002Control Supplement  
1/15/1974 000Approval  
 
Therapeutic Equivalents
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