Visitor Monitoring Drug History: AQUAMEPHYTON
 
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: AQUAMEPHYTON
FDA Application No: (NDA) 012223
Active Ingredient(s): PHYTONADIONE
Company: ATON
 
Label History
 
Labels are not available on this site for AQUAMEPHYTON, (NDA) 012223
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/4/2003 039Labeling Revision Letter 
2/27/2003 038Labeling Revision Letter 
8/16/2001 037Control Supplement  
5/18/2001 036Labeling Revision Letter 
7/14/1998 035Control Supplement  
5/28/1998 034Control Supplement  
1/14/1997 033Control Supplement  
12/6/1996 032Control Supplement  
12/6/1996 031Control Supplement  
6/25/1996 030Manufacturing Change or Addition  
12/5/1995 029Manufacturing Change or Addition  
6/8/1995 028Package Change  
4/24/1995 027Labeling Revision  
6/28/1991 026Labeling Revision  
4/26/1990 025Labeling Revision  
8/27/1985 024Package Change  
10/11/1984 023Package Change  
8/18/1982 022Labeling Revision  
8/19/1986 021Practioner Draft Labeling  
7/14/1981 020Package Change  
11/3/1981 019Manufacturing Change or Addition  
11/28/1980 018Control Supplement  
9/18/1979 017Control Supplement  
9/1/1976 016Control Supplement  
6/28/1960 000Approval  
 
Therapeutic Equivalents
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