Visitor Monitoring Drug History: OMNIPAQUE 350
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
Label and Approval History

Drug Name: OMNIPAQUE 350
FDA Application No: (NDA) 020608
Active Ingredient(s): IOHEXOL
Company: GE HEALTHCARE
 
Label History
 
Labels are not available on this site for OMNIPAQUE 350, (NDA) 020608
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/1/2007 018Labeling Revision Letter 
2/10/2004 010Labeling Revision Letter 
3/5/2004 009Labeling Revision Letter 
11/20/2002 005Manufacturing Change or Addition  
8/5/2002 004Manufacturing Change or Addition  
12/19/2000 003Control Supplement  
6/4/1997 002Manufacturing Change or Addition  
3/10/1998 001Labeling Revision  
10/24/1995 000Approval  
 
Therapeutic Equivalents
©2019 Drugs That Causes a False Positive on a Drug Test