Visitor Monitoring Drug History: ULTRAVIST 240
 
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: ULTRAVIST 240
FDA Application No: (NDA) 020220
Active Ingredient(s): IOPROMIDE
Company: BAYER HLTHC
 
Label History
 
View the label approved on September 4, 2007 for ULTRAVIST 240, (NDA) 020220


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
8/31/2007 027Labeling Revision Letter
Label 
8/12/2005 022Labeling Revision Letter 
3/12/2004 018Package Change Letter
Label 
10/30/2002 014Manufacturing Change or Addition  
4/11/2002 013Manufacturing Change or Addition  
11/5/2001 012Manufacturing Change or Addition  
1/4/2001 011Package Change  
10/24/2000 010Manufacturing Change or Addition  
9/27/2000 009Control Supplement  
4/25/2003 008Labeling Revision Letter 
12/27/1999 007Manufacturing Change or Addition  
11/25/1998 006Control Supplement  
11/3/1998 005Control Supplement  
6/5/1997 004Control Supplement  
7/23/1997 002Patient Population Altered  
5/30/1995 001Labeling Revision  
5/10/1995 000Approval  
 
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