Visitor Monitoring Drug History: NATRECOR
 
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: NATRECOR
FDA Application No: (NDA) 020920
Active Ingredient(s): NESIRITIDE RECOMBINANT
Company: SCIOS
 
Label History
 
View the label approved on April 16, 2007 for NATRECOR, (NDA) 020920


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
11/30/2006 012Labeling Revision Letter
Label 
4/20/2005 008Labeling Revision Letter
Label 
4/29/2005 006Labeling Revision Letter 
7/2/2004 003Labeling Revision Letter 
8/10/2001 000Approval Letter
Label
Review
Consumer Information Sheet 
 
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