Visitor Monitoring Drug History: MELLARIL
 
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: MELLARIL
FDA Application No: (NDA) 011808
Active Ingredient(s): THIORIDAZINE HYDROCHLORIDE
Company: NOVARTIS
 
Label History
 
Labels are not available on this site for MELLARIL, (NDA) 011808
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/28/2001 179Manufacturing Change or Addition  
3/15/2001 178Labeling Revision Letter 
6/15/2001 177Manufacturing Change or Addition  
3/1/2000 176Manufacturing Change or Addition  
6/19/2000 175Labeling Revision  
4/15/1999 173Package Change  
5/25/1999 172Expiration Date Change  
1/15/1997 170Control Supplement  
3/20/1996 169Control Supplement  
11/22/1995 168Manufacturing Change or Addition  
10/17/1995 165Control Supplement  
12/2/1994 138Formulation Revision  
11/28/1994 117Control Supplement  
3/15/1962 000Approval  
 
There are no Therapeutic Equivalents
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