Visitor Monitoring Drug History: NAPROXEN
 
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Label and Approval History

Drug Name: NAPROXEN
FDA Application No: (ANDA) 075061
Active Ingredient(s): NAPROXEN
Company: SANDOZ
 
Label History
 
Labels are not available on this site for NAPROXEN, (ANDA) 075061
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/10/2002 005Package Change  
5/10/2002 004Facility Addition  
10/3/2001 003Supplier Addition  
10/3/2001 002Control Supplement  
8/2/2000 001Supplier Addition  
2/18/1998 000Approval Review 
 
Therapeutic Equivalents
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