Visitor Monitoring Drug History: TELEPAQUE
 
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: TELEPAQUE
FDA Application No: (NDA) 008032
Active Ingredient(s): IOPANOIC ACID
Company: GE HEALTHCARE
 
Label History
 
Labels are not available on this site for TELEPAQUE, (NDA) 008032
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/2/1990 023Control Supplement  
5/20/1987 022Control Supplement  
7/1/1986 021Labeling Revision  
11/23/1985 020Labeling Revision  
4/19/1985 019Labeling Revision  
3/14/1984 018Practioner Draft Labeling  
9/30/1983 017Package Change  
11/27/1979 015Labeling Revision  
10/12/1978 013Labeling Revision  
10/15/1976 012Control Supplement  
10/15/1976 011Labeling Revision  
10/15/1976 010Labeling Revision  
10/18/1976 009Labeling Revision  
7/16/1951 000Approval  
 
There are no Therapeutic Equivalents
©2019 Drugs That Causes a False Positive on a Drug Test