Visitor Monitoring Drug History: FERROUS CITRATE FE 59
 
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Label and Approval History

Drug Name: FERROUS CITRATE FE 59
FDA Application No: (NDA) 016729
Active Ingredient(s): FERROUS CITRATE, FE-59
Company: MALLINCKRODT
 
Label History
 
Labels are not available on this site for FERROUS CITRATE FE 59, (NDA) 016729
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/24/1984 009Practioner Draft Labeling  
5/10/1982 007Control Supplement  
8/23/1977 004Manufacturing Change or Addition  
7/27/1977 003Manufacturing Change or Addition  
12/17/1973 000Approval  
 
There are no Therapeutic Equivalents
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