Visitor Monitoring Drug History: HYPAQUE
 
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: HYPAQUE
FDA Application No: (NDA) 011386
Active Ingredient(s): DIATRIZOATE SODIUM
Company: GE HEALTHCARE
 
Label History
 
Labels are not available on this site for HYPAQUE, (NDA) 011386
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/30/1994 034Manufacturing Change or Addition  
6/15/1995 033Labeling Revision  
8/23/1996 032Control Supplement  
10/5/1993 031Manufacturing Change or Addition  
8/1/1990 029Manufacturing Change or Addition  
8/1/1990 028Package Change  
5/9/1988 027Labeling Revision  
8/2/1988 026Control Supplement  
8/14/1986 025Manufacturing Change or Addition  
3/17/1986 024Labeling Revision  
2/10/1986 023Labeling Revision  
12/28/1984 022Labeling Revision  
9/12/1984 021Labeling Revision  
5/29/1991 019Package Change  
6/30/1982 016Labeling Revision  
1/12/1984 015Labeling Revision  
7/5/1979 014Manufacturing Change or Addition  
12/13/1977 013Labeling Revision  
9/29/1976 011Labeling Revision  
3/26/1956 000Approval  
 
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