Visitor Monitoring Drug Details: CYTOXAN
 
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Drug Details

Drug Name: CYTOXAN
FDA Application No: (NDA) 012142
Active Ingredient(s): CYCLOPHOSPHAMIDE
Company: BRISTOL MYERS SQUIBB
Original Approval or Tentative Approval Date: November 16, 1959
Chemical Type: 2 New active ingredient
Review Classification: P Priority review drug
 
Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
CYTOXAN CYCLOPHOSPHAMIDE100MG/VIALINJECTABLE; INJECTION Discontinued No None
CYTOXAN CYCLOPHOSPHAMIDE200MG/VIALINJECTABLE; INJECTION Discontinued No None
CYTOXAN CYCLOPHOSPHAMIDE500MG/VIALINJECTABLE; INJECTION Discontinued No None
CYTOXAN CYCLOPHOSPHAMIDE1GM/VIALINJECTABLE; INJECTION Discontinued No None
CYTOXAN CYCLOPHOSPHAMIDE2GM/VIALINJECTABLE; INJECTION Discontinued No None
LYOPHILIZED CYTOXAN CYCLOPHOSPHAMIDE100MG/VIALINJECTABLE; INJECTION Prescription Yes AP
LYOPHILIZED CYTOXAN CYCLOPHOSPHAMIDE200MG/VIALINJECTABLE; INJECTION Prescription Yes AP
LYOPHILIZED CYTOXAN CYCLOPHOSPHAMIDE500MG/VIALINJECTABLE; INJECTION Prescription Yes AP
LYOPHILIZED CYTOXAN CYCLOPHOSPHAMIDE2GM/VIALINJECTABLE; INJECTION Prescription Yes AP
LYOPHILIZED CYTOXAN CYCLOPHOSPHAMIDE1GM/VIALINJECTABLE; INJECTION Prescription Yes AP


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