Visitor Monitoring Drug History: CYTOXAN
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: CYTOXAN
FDA Application No: (NDA) 012141
Active Ingredient(s): CYCLOPHOSPHAMIDE
Company: BRISTOL MYERS SQUIBB
 
Label History
 
Labels are not available on this site for CYTOXAN, (NDA) 012141
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/27/2003 087Labeling Revision Letter 
1/30/2001 086Labeling Revision  
8/20/1999 085Manufacturing Change or Addition  
5/28/1999 084Labeling Revision  
6/15/2000 083Labeling Revision  
12/20/1995 081Labeling Revision  
4/29/1987 077Manufacturing Change or Addition  
7/11/1986 075Labeling Revision  
7/11/1986 074Labeling Revision  
7/11/1986 073Labeling Revision  
7/11/1986 072Labeling Revision  
1/15/1986 071Labeling Revision  
12/4/1985 070Labeling Revision  
8/30/1985 069Manufacturing Change or Addition  
12/5/1985 067Formulation Revision  
8/10/1984 066Control Supplement  
3/15/1983 065Labeling Revision  
3/4/1982 064Package Change  
4/29/1987 063Practioner Draft Labeling  
7/28/1982 062Control Supplement  
9/27/1980 061Labeling Revision  
2/27/1981 060Control Supplement  
8/3/1979 059Control Supplement  
5/24/1979 058Package Change  
1/25/1980 057Manufacturing Change or Addition  
4/30/1979 056Manufacturing Change or Addition  
8/28/1978 055Control Supplement  
8/16/1978 054Supplement  
11/27/1978 053Manufacturing Change or Addition  
7/19/1978 052Control Supplement  
5/23/1978 051Control Supplement  
11/16/1977 050Manufacturing Change or Addition  
11/16/1977 049Labeling Revision  
4/25/1977 048Control Supplement  
8/8/1978 047Control Supplement  
5/16/1977 046Manufacturing Change or Addition  
3/17/1977 045Control Supplement  
10/18/1976 044Control Supplement  
11/1/1976 042Labeling Revision  
6/9/1976 041Control Supplement  
6/9/1976 040Control Supplement  
3/17/1977 039Manufacturing Change or Addition  
4/29/1987 037New or Modified Indication  
10/18/1976 035Other Amendment  
11/16/1959 000Approval  
 
Therapeutic Equivalents
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