Visitor Monitoring Drug History: TEGISON
 
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: TEGISON
FDA Application No: (NDA) 019369
Active Ingredient(s): ETRETINATE
Company: ROCHE
 
Label History
 
Labels are not available on this site for TEGISON, (NDA) 019369
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/16/1995 011Control Supplement  
1/12/1994 010Manufacturing Change or Addition  
10/8/1991 008Control Supplement  
10/16/1990 007Control Supplement  
8/31/1988 006Control Supplement  
8/5/1988 005Expiration Date Change  
3/25/1988 004Package Change  
5/27/1988 003Labeling Revision  
4/2/1987 002Control Supplement  
4/29/1987 001Labeling Revision  
9/30/1986 000Approval  
 
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