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) 075416
Active Ingredient(s): NAPROXEN SODIUM
Company: ANDRX PHARMS
 
Label History
 
Labels are not available on this site for NAPROXEN SODIUM, (ANDA) 075416
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/23/2003 003Control Supplement  
4/23/2003 002Labeling  
3/21/2003 001Control Supplement  
4/3/2007 0006Labeling  
8/27/2002 000Approval  
3/17/2000 000Tentative Approval  
7/5/2001 000Tentative Approval  
 
Therapeutic Equivalents
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