Visitor Monitoring Drug History: ENDRATE
 
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Label and Approval History

Drug Name: ENDRATE
FDA Application No: (NDA) 011355
Active Ingredient(s): EDETATE DISODIUM
Company: HOSPIRA
 
Label History
 
Labels are not available on this site for ENDRATE, (NDA) 011355
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/2/2001 013Expiration Date Change  
3/19/1999 012Labeling Revision  
10/31/1997 011Labeling Revision  
8/30/1996 010Control Supplement  
2/8/1985 008Labeling Revision  
2/26/1985 007Practioner Draft Labeling  
11/25/1981 006Control Supplement  
2/25/1981 005Labeling Revision  
2/16/1959 000Approval  
 
Therapeutic Equivalents
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