Visitor Monitoring Drug History: OPTISON
 
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: OPTISON
FDA Application No: (NDA) 020899
Active Ingredient(s): ALBUMIN HUMAN
Company: GE HEALTHCARE
 
Label History
 
View the label approved on October 4, 2007 for OPTISON, (NDA) 020899


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
5/10/2002 007Manufacturing Change or Addition Letter
Label 
12/18/2000 006Manufacturing Change or Addition  
5/6/1999 005Manufacturing Change or Addition  
2/4/2000 004Manufacturing Change or Addition  
3/14/2000 003Labeling Revision  
2/1/1999 002Manufacturing Change or Addition  
7/31/1998 001Manufacturing Change or Addition  
12/31/1997 000Approval  
 
There are no Therapeutic Equivalents
©2019 Drugs That Causes a False Positive on a Drug Test