Visitor Monitoring Drug History: DARVON W/ ASA
 
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 W/ ASA
FDA Application No: (NDA) 010996
Active Ingredient(s): ASPIRIN; PROPOXYPHENE HYDROCHLORIDE
Company: XANODYNE PHARM
 
Label History
 
Labels are not available on this site for DARVON W ASA, (NDA) 010996
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/27/2004 068Manufacturing Change or Addition Letter 
2/24/1999 065Manufacturing Change or Addition  
10/5/1998 064Manufacturing Change or Addition  
8/10/1998 063Control Supplement  
4/6/1998 062Package Change  
8/1/2002 061Labeling Revision Letter 
9/15/1992 060Package Change  
9/2/1994 058Labeling Revision  
9/15/1992 057Control Supplement  
8/23/1994 055Labeling Revision  
4/16/1987 048Control Supplement  
12/16/1986 047Control Supplement  
7/16/1986 042Labeling Revision  
9/2/1986 041Manufacturing Change or Addition  
4/21/1986 040Labeling Revision  
4/21/1986 037Labeling Revision  
1/28/1985 036Control Supplement  
3/8/1983 035Formulation Revision  
10/28/1981 034Labeling Revision  
10/28/1981 033Labeling Revision  
5/20/1981 032Labeling Revision  
4/16/1980 031Labeling Revision  
9/26/1979 030Labeling Revision  
7/17/1979 029Final Printed Labeling - MarkIV  
3/26/1979 028Labeling Revision  
10/13/1978 027Package Change  
5/26/1978 026Expiration Date Change  
1/18/1980 024Control Supplement  
5/3/1977 023Package Change  
5/3/1977 022Package Change  
7/23/1976 020Labeling Revision  
1/6/1975 014Labeling Revision  
11/12/1957 000Approval  
 
There are no Therapeutic Equivalents
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