Visitor Monitoring Drug History: HEXABRIX
 
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: HEXABRIX
FDA Application No: (NDA) 018905
Active Ingredient(s): IOXAGLATE MEGLUMINE; IOXAGLATE SODIUM
Company: MALLINCKRODT
 
Label History
 
Labels are not available on this site for HEXABRIX, (NDA) 018905
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/23/2001 022Package Change  
10/27/1999 021Formulation Revision  
4/26/1995 020Manufacturing Change or Addition  
1/13/1995 019Labeling Revision  
8/28/1992 017Package Change  
3/17/1994 016Control Supplement  
12/4/1992 015Control Supplement  
3/30/1994 014Manufacturing Change or Addition  
3/30/1990 013Control Supplement  
7/3/1989 012Labeling Revision  
1/31/1989 010Manufacturing Change or Addition  
10/10/1989 007Package Change  
12/30/1986 006Labeling Revision  
11/21/1986 004Labeling Revision  
10/22/1986 002New or Modified Indication  
6/3/1988 001Package Change  
7/26/1985 000Approval  
 
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