Visitor Monitoring Drug History: ESTRACE
 
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Label and Approval History

Drug Name: ESTRACE
FDA Application No: (ANDA) 084500
Active Ingredient(s): ESTRADIOL
Company: BRISTOL MYERS SQUIBB
 
Label History
 
Labels are not available on this site for ESTRACE, (ANDA) 084500
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
1/25/2001 041Control Supplement  
10/5/1998 039Labeling  
7/28/1997 038Chemistry  
1/8/1997 037Labeling  
9/11/1995 036Chemistry  
1/19/1995 035Chemistry  
1/19/1995 034Chemistry  
1/19/1995 033Chemistry  
1/19/1995 032Chemistry  
5/9/1994 031Labeling  
1/12/1993 030Labeling in Effect  
8/10/1992 029Labeling  
7/18/1989 027Chemistry  
7/18/1989 026Chemistry  
11/9/1992 025Chemistry  
11/9/1992 024Labeling  
11/9/1992 023Chemistry  
9/8/1992 022Labeling  
12/19/1985 021Chemistry  
3/10/1983 017Chemistry  
6/7/1982 014Chemistry  
7/23/1975 000Approval  
 
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