Visitor Monitoring Drug History: VASCORAY
 
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: VASCORAY
FDA Application No: (NDA) 016783
Active Ingredient(s): IOTHALAMATE MEGLUMINE; IOTHALAMATE SODIUM
Company: MALLINCKRODT
 
Label History
 
Labels are not available on this site for VASCORAY, (NDA) 016783
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/13/1995 029Labeling Revision  
8/28/1992 028Package Change  
12/4/1992 027Control Supplement  
3/30/1990 026Control Supplement  
6/28/1989 025Labeling Revision  
12/1/1989 024Control Supplement  
8/19/1988 023Control Supplement  
4/23/1985 022Labeling Revision  
10/10/1989 021Package Change  
12/4/1984 020Control Supplement  
6/25/1984 019Manufacturing Change or Addition  
8/3/1983 018Labeling Revision  
6/16/1982 017Package Change  
1/25/1979 015Control Supplement  
10/18/1978 014General Efficacy (MarkIV)  
5/14/1976 012Labeling Revision  
5/10/1976 011Control Supplement  
1/23/1976 010Control Supplement  
1/23/1976 009Control Supplement  
7/30/1975 008Control Supplement  
1/26/1971 000Approval  
 
There are no Therapeutic Equivalents
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