Visitor Monitoring Drug History: RESCRIPTOR
 
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: RESCRIPTOR
FDA Application No: (NDA) 020705
Active Ingredient(s): DELAVIRDINE MESYLATE
Company: AGOURON
 
Label History
 
View the label approved on April 22, 2003 for RESCRIPTOR, (NDA) 020705


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
4/7/2006 010Labeling Revision Letter 
3/14/2002 009Labeling Revision Letter
Review 
5/16/2001 008Accelerated Approval Label
Review 
8/16/1999 004Labeling Revision Review 
7/14/1999 003Formulation Revision Letter
Label
Review 
10/23/1998 002Manufacturing Change or Addition Review 
2/11/1998 001Labeling Revision  
4/4/1997 000Approval  
 
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