Visitor Monitoring Drug History: TALWIN 50
 
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Label and Approval History

Drug Name: TALWIN 50
FDA Application No: (NDA) 016732
Active Ingredient(s): PENTAZOCINE HYDROCHLORIDE
Company: SANOFI AVENTIS US
 
Label History
 
Labels are not available on this site for TALWIN 50, (NDA) 016732
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/19/1982 051Package Change  
10/2/1981 047Labeling Revision  
1/9/1981 046Package Change  
10/2/1980 045Expiration Date Change  
8/19/1980 044Package Change  
9/5/1979 043Labeling Revision  
7/23/1979 042Labeling Revision  
5/31/1979 041Labeling Revision  
4/30/1979 040Labeling Revision  
4/11/1979 039Labeling Revision  
11/6/1978 038Manufacturing Change or Addition  
11/28/1978 037Package Change  
11/28/1977 036Manufacturing Change or Addition  
8/30/1977 035Labeling Revision  
5/11/1977 034Manufacturing Change or Addition  
7/16/1976 033Labeling Revision  
10/31/1975 030Labeling Revision  
7/30/1975 029Control Supplement  
7/30/1975 028Control Supplement  
4/3/1975 027Control Supplement  
9/26/1974 026Labeling Revision  
12/9/1974 025Distributor  
11/8/1974 022Labeling Revision  
2/3/1969 000Approval  
 
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