Visitor Monitoring Drug History: TAVIST-D
 
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: TAVIST-D
FDA Application No: (NDA) 018298
Active Ingredient(s): CLEMASTINE FUMARATE; PHENYLPROPANOLAMINE HYDROCHLORIDE
Company: NOVARTIS
 
Label History
 
Labels are not available on this site for TAVISTD, (NDA) 018298
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/31/1996 024New or Modified Indication  
6/16/1995 022Package Change  
11/7/1995 021Package Change  
2/3/1995 019Labeling Revision  
7/21/1994 018Control Supplement  
2/12/1992 014Control Supplement  
12/4/1987 013Control Supplement  
2/12/1992 011Labeling Revision  
2/12/1992 010Control Supplement  
5/15/1986 008Labeling Revision  
9/12/1986 006Control Supplement  
4/3/1986 004Control Supplement  
8/21/1992 003OTC Labeling  
2/20/1985 002Control Supplement  
3/2/1983 001Control Supplement  
12/15/1982 000Approval  
 
There are no Therapeutic Equivalents
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