Visitor Monitoring Drug History: TESSALON
 
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: TESSALON
FDA Application No: (NDA) 011210
Active Ingredient(s): BENZONATATE
Company: FOREST LABS
 
Label History
 
Labels are not available on this site for TESSALON, (NDA) 011210
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/23/2002 041Manufacturing Change or Addition  
11/1/2000 040Control Supplement  
6/30/2000 039Control Supplement  
6/8/1999 037Manufacturing Change or Addition  
6/25/1999 035Manufacturing Change or Addition  
12/1/1993 032Manufacturing Change or Addition  
9/4/1992 031Labeling Revision  
10/8/1986 030Labeling Revision  
11/29/1985 029Practioner Draft Labeling  
11/5/1985 027Control Supplement  
6/13/1985 026Control Supplement  
11/29/1985 025Labeling Revision  
7/15/1981 022Manufacturing Change or Addition  
7/3/1980 021Control Supplement  
8/28/1979 020Manufacturing Change or Addition  
7/6/1979 019Expiration Date Change  
9/29/1978 018Labeling Revision  
9/29/1978 015Control Supplement  
10/24/1978 014Control Supplement  
3/31/1975 013Control Supplement  
12/30/1974 011Supplement  
4/12/1972 002Labeling Revision  
2/10/1958 000Approval  
 
Therapeutic Equivalents
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