Visitor Monitoring Drug History: ULTIVA
 
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: ULTIVA
FDA Application No: (NDA) 020630
Active Ingredient(s): REMIFENTANIL HYDROCHLORIDE
Company: ABBOTT
 
Label History
 
View the label approved on April 5, 2004 for ULTIVA, (NDA) 020630


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
10/3/2002 009Manufacturing Change or Addition  
12/20/2002 008Manufacturing Change or Addition  
11/19/2001 007Manufacturing Change or Addition  
9/19/2000 006Control Supplement  
3/8/2004 005Patient Population Altered Letter
Label 
6/23/1999 003Labeling Revision  
11/23/1999 002Efficacy Supplement with Clinical Data to Support  
10/15/1999 001Patient Population Altered  
7/12/1996 000Approval  
 
There are no Therapeutic Equivalents
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