Visitor Monitoring Drug History: NAPROXEN SODIUM
 
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: NAPROXEN SODIUM
FDA Application No: (ANDA) 074635
Active Ingredient(s): NAPROXEN SODIUM
Company: LEINER
 
Label History
 
Labels are not available on this site for NAPROXEN SODIUM, (ANDA) 074635
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/4/2002 015Facility Addition  
4/29/2002 014Manufacturing Revision  
4/29/2002 013Control Supplement  
9/21/2000 012Facility Addition  
8/2/2000 010Facility Addition  
8/24/1999 008Labeling  
3/3/2000 007Control Supplement  
3/3/2000 006Manufacturing Revision  
2/11/1999 005Chemistry  
2/11/1999 004Chemistry  
4/28/1998 003Chemistry  
12/7/1998 002Chemistry  
4/14/1999 001Chemistry  
1/13/1997 000Approval  
8/20/1996 000Tentative Approval  
 
Therapeutic Equivalents
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