Visitor Monitoring Drug History: NAPRELAN
 
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: NAPRELAN
FDA Application No: (NDA) 020353
Active Ingredient(s): NAPROXEN SODIUM
Company: STAT TRADE
 
Label History
 
View the label approved on January 20, 2006 for NAPRELAN, (NDA) 020353


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
5/29/2007 019Labeling Revision Letter 
1/18/2006 016Labeling Revision Letter
Label 
4/15/2002 014Control Supplement  
10/2/2001 013Manufacturing Change or Addition  
6/4/2001 012Package Change  
6/15/2000 011Control Supplement  
2/15/2000 010Package Change  
7/20/1999 009Package Change  
2/4/2002 008Labeling Revision  
11/2/1999 007Control Supplement  
12/23/1997 006Package Change  
5/12/1997 005Expiration Date Change  
1/31/1997 004Expiration Date Change  
1/31/1997 003Control Supplement  
3/28/1996 001Labeling Revision Review 
1/5/1996 000Approval  
 
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