Visitor Monitoring Drug History: TENORMIN
 
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: TENORMIN
FDA Application No: (NDA) 018240
Active Ingredient(s): ATENOLOL
Company: ASTRAZENECA
 
Label History
 
Labels are not available on this site for TENORMIN, (NDA) 018240
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
2/9/2005 029Labeling Revision Letter 
11/6/2003 028Labeling Revision Letter 
1/9/2003 027Labeling Revision Letter 
7/21/1999 026Labeling Revision Review 
4/4/2000 025Labeling Revision Review 
10/11/1996 024Package Change  
2/9/1996 023Labeling Revision  
5/4/1994 021Labeling Revision  
4/29/1993 020Labeling Revision  
8/5/1992 019Labeling Revision  
8/5/1992 018Labeling Revision  
9/18/1991 017Labeling Revision  
2/21/1991 016Labeling Revision  
2/21/1991 015Labeling Revision  
2/21/1991 014Labeling Revision  
4/9/1990 013New Dosage Regimen  
2/13/1987 011Package Change  
9/18/1985 009Labeling Revision  
11/19/1984 008Control Supplement  
7/12/1984 007Manufacturing Change or Addition  
12/15/1983 006Control Supplement  
9/13/1989 005New or Modified Indication  
9/27/1983 004Package Change  
4/7/1983 003Formulation Revision  
9/4/1985 002New or Modified Indication  
9/23/1981 001Labeling Revision  
8/19/1981 000Approval  
 
Therapeutic Equivalents
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