Visitor Monitoring Drug History: CEENU
 
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: CEENU
FDA Application No: (NDA) 017588
Active Ingredient(s): LOMUSTINE
Company: BRISTOL MYERS SQUIBB
 
Label History
 
Labels are not available on this site for CEENU, (NDA) 017588
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/27/2003 033Labeling Revision Letter 
6/1/1999 032Manufacturing Change or Addition  
12/20/2002 031Labeling Revision Letter 
3/2/1993 030Control Supplement  
8/1/1990 029Control Supplement  
11/14/1988 028Manufacturing Change or Addition  
3/14/1991 027Control Supplement  
7/5/1988 026Control Supplement  
8/26/1987 025Manufacturing Change or Addition  
9/12/1986 024Manufacturing Change or Addition  
9/12/1986 023Manufacturing Change or Addition  
9/22/1986 022Labeling Revision  
9/22/1986 020Labeling Revision  
6/18/1985 019Manufacturing Change or Addition  
3/6/1985 017Control Supplement  
6/28/1983 015Labeling Revision  
7/22/1983 012Labeling Revision  
10/14/1986 011Practioner Draft Labeling  
2/16/1982 010Labeling Revision  
11/12/1980 009Package Change  
11/12/1980 008Labeling Revision  
8/7/1980 007Expiration Date Change  
9/19/1980 005Formulation Revision  
11/14/1978 004Labeling Revision  
4/22/1977 002Control Supplement  
8/4/1976 000Approval  
 
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