Visitor Monitoring Drug History: RENESE
 
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: RENESE
FDA Application No: (NDA) 012845
Active Ingredient(s): POLYTHIAZIDE
Company: PFIZER
 
Label History
 
Labels are not available on this site for RENESE, (NDA) 012845
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/24/1998 026Labeling Revision  
6/26/1992 025Manufacturing Change or Addition  
3/20/1984 024Package Change  
2/7/1984 023Package Change  
2/5/1981 021Package Change  
4/6/1979 020Control Supplement  
5/22/1978 019Package Change  
10/6/1977 018Control Supplement  
9/28/1976 017Labeling Revision  
9/28/1976 016Formulation Revision  
10/28/1975 014Control Supplement  
6/5/1975 013Control Supplement  
5/7/1975 012Labeling Revision  
9/26/1961 000Approval  
 
There are no Therapeutic Equivalents
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