Visitor Monitoring Drug History: TALWIN NX
 
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 NX
FDA Application No: (NDA) 018733
Active Ingredient(s): NALOXONE HYDROCHLORIDE; PENTAZOCINE HYDROCHLORIDE
Company: SANOFI AVENTIS US
 
Label History
 
Labels are not available on this site for TALWIN NX, (NDA) 018733
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/26/2003 012Labeling Revision Letter 
2/29/1988 011Manufacturing Change or Addition  
1/12/1989 010Labeling Revision  
2/2/1987 009Manufacturing Change or Addition  
10/9/1985 008Labeling Revision  
1/12/1989 007Labeling Revision  
4/5/1983 006Manufacturing Change or Addition  
4/5/1983 005Control Supplement  
4/5/1983 004Control Supplement  
4/5/1983 003Control Supplement  
4/5/1983 002Package Change  
4/5/1983 001Package Change  
12/16/1982 000Approval  
 
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