Visitor Monitoring Drug History: TALWIN
 
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: TALWIN
FDA Application No: (NDA) 016194
Active Ingredient(s): PENTAZOCINE LACTATE
Company: HOSPIRA
 
Label History
 
Labels are not available on this site for TALWIN, (NDA) 016194
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/27/2004 068Control Supplement Letter 
9/26/2001 065Control Supplement  
1/31/2001 064Control Supplement  
6/27/2000 063Control Supplement  
5/24/2000 062Labeling Revision  
10/22/1998 061Efficacy Supplement with Clinical Data to Support  
10/10/1995 060Control Supplement  
4/21/1993 059Control Supplement  
9/29/1992 058Control Supplement  
1/25/1990 057Manufacturing Change or Addition  
8/23/1989 056Labeling Revision  
9/22/1989 055Control Supplement  
5/4/1988 053Control Supplement  
3/30/1988 052Labeling Revision  
7/15/1985 049Expiration Date Change  
8/24/1983 048Package Change  
9/1/1983 047Package Change  
5/18/1983 045Labeling Revision  
3/18/1981 044Manufacturing Change or Addition  
9/29/1981 043Labeling Revision  
8/7/1981 042Formulation Revision  
11/5/1980 041Control Supplement  
10/9/1981 040Labeling Revision  
4/9/1979 039Labeling Revision  
7/18/1978 038Control Supplement  
9/14/1978 037Labeling Revision  
7/21/1978 036Labeling Revision  
1/4/1977 035Formulation Revision  
12/16/1977 034Manufacturing Change or Addition  
12/2/1977 033Manufacturing Change or Addition  
2/22/1978 032Labeling Revision  
12/15/1977 031Manufacturing Change or Addition  
6/7/1976 030Manufacturing Change or Addition  
7/16/1976 028Labeling Revision  
3/26/1976 027Control Supplement  
10/23/1975 025Labeling Revision  
10/25/1974 024Labeling Revision  
2/6/1974 021Labeling Revision  
3/26/1976 018Control Supplement  
7/24/1967 000Approval  
 
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