Visitor Monitoring Drug History: MATULANE
 
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: MATULANE
FDA Application No: (NDA) 016785
Active Ingredient(s): PROCARBAZINE HYDROCHLORIDE
Company: SIGMA TAU
 
Label History
 
View the label approved on April 17, 2003 for MATULANE, (NDA) 016785


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/20/2002 035Labeling Revision Letter 
3/13/2002 034Manufacturing Change or Addition  
11/13/2001 033Expiration Date Change  
3/2/2001 032Control Supplement  
3/8/1999 031Control Supplement  
10/16/1998 030Control Supplement  
4/9/1987 029Labeling Revision  
5/7/1986 028Labeling Revision  
3/5/1987 027Manufacturing Change or Addition  
8/17/1987 026Labeling Revision  
4/29/1986 024Practioner Draft Labeling  
12/18/1981 023Formulation Revision  
3/31/1981 022Manufacturing Change or Addition  
7/24/1980 021Formulation Revision  
11/14/1979 020Package Change  
8/11/1981 019Labeling Revision  
3/24/1980 018Labeling Revision  
1/9/1979 017Control Supplement  
11/27/1978 016Control Supplement  
5/16/1977 014Control Supplement  
4/8/1976 013Control Supplement  
7/22/1969 000Approval Label 
 
There are no Therapeutic Equivalents
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