Visitor Monitoring Drug History: TALACEN
 
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: TALACEN
FDA Application No: (NDA) 018458
Active Ingredient(s): ACETAMINOPHEN; PENTAZOCINE HYDROCHLORIDE
Company: SANOFI AVENTIS US
 
Label History
 
Labels are not available on this site for TALACEN, (NDA) 018458
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/10/2003 012Labeling Revision Letter 
10/31/2000 010Labeling Revision  
3/30/2000 009Control Supplement  
3/2/1988 008Manufacturing Change or Addition  
11/10/1988 007Labeling Revision  
5/22/1987 006Labeling Revision  
3/27/1987 005Labeling Revision  
10/25/1985 004Labeling Revision  
5/7/1985 003Labeling Revision  
6/26/1984 002Labeling Revision  
1/24/1984 001Labeling Revision  
9/23/1982 000Approval  
 
There are no Therapeutic Equivalents
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