Visitor Monitoring Drug Details: IFEX
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Drug Details

Drug Name: IFEX
FDA Application No: (NDA) 019763
Active Ingredient(s): IFOSFAMIDE
Company: BRISTOL MYERS SQUIBB
Original Approval or Tentative Approval Date: December 30, 1988
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
O Orphan drug
 
Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
IFEX IFOSFAMIDE1GM/VIALINJECTABLE; INJECTION Discontinued No None
IFEX IFOSFAMIDE3GM/VIALINJECTABLE; INJECTION Discontinued No None
IFEX/MESNEX KIT IFOSFAMIDE; MESNA1GM/VIAL; 100MG/MLINJECTABLE; INJECTION Prescription Yes None
IFEX/MESNEX KIT IFOSFAMIDE; MESNA3GM/VIAL; 100MG/MLINJECTABLE; INJECTION Prescription Yes None


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