Visitor Monitoring Drug History: DARVON
 
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: DARVON
FDA Application No: (NDA) 010997
Active Ingredient(s): PROPOXYPHENE HYDROCHLORIDE
Company: XANODYNE PHARM
 
Label History
 
Labels are not available on this site for DARVON, (NDA) 010997
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/24/1999 047Manufacturing Change or Addition  
10/5/1998 046Manufacturing Change or Addition  
8/10/1998 045Control Supplement  
4/2/1998 044Package Change  
8/1/2002 043Labeling Revision Letter 
9/2/1994 042Labeling Revision  
9/15/1992 041Control Supplement  
8/23/1994 040Labeling Revision  
12/8/1986 035Control Supplement  
10/16/1986 033Labeling Revision  
11/5/1986 032Control Supplement  
4/21/1986 031Labeling Revision  
4/21/1986 028Labeling Revision  
4/21/1986 027Labeling Revision  
1/28/1985 026Control Supplement  
10/28/1981 025Labeling Revision  
5/20/1981 024Labeling Revision  
8/10/1981 023Formulation Revision  
4/15/1980 022Labeling Revision  
9/26/1979 021Labeling Revision  
10/13/1978 020Package Change  
5/26/1978 019Formulation Revision  
2/27/1979 018Expiration Date Change  
1/21/1980 016Control Supplement  
5/3/1977 015Package Change  
5/3/1977 014Package Change  
7/23/1976 013Labeling Revision  
1/6/1975 010Labeling Revision  
8/16/1957 000Approval  
 
Therapeutic Equivalents
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