Visitor Monitoring Drug Details: FERROUS CITRATE FE 59
 
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Drug Details

Drug Name: FERROUS CITRATE FE 59
FDA Application No: (NDA) 016729
Active Ingredient(s): FERROUS CITRATE, FE-59
Company: MALLINCKRODT
Original Approval or Tentative Approval Date: December 17, 1973
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
FERROUS CITRATE FE 59 FERROUS CITRATE, FE-5925uCi/MLINJECTABLE; INJECTION Discontinued No None


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