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) 074646
Active Ingredient(s): NAPROXEN SODIUM
Company: SANDOZ
 
Label History
 
Labels are not available on this site for NAPROXEN SODIUM, (ANDA) 074646
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/22/2000 002Control Supplement  
2/22/2000 001Supplier Addition  
1/13/1997 000Approval  
12/10/1996 000Tentative Approval  
 
Therapeutic Equivalents
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