Visitor Monitoring Drug History: DIUCARDIN
 
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Label and Approval History

Drug Name: DIUCARDIN
FDA Application No: (ANDA) 083383
Active Ingredient(s): HYDROFLUMETHIAZIDE
Company: WYETH AYERST
 
Label History
 
Labels are not available on this site for DIUCARDIN, (ANDA) 083383
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/28/1990 014Labeling  
12/28/1990 013Labeling  
1/18/1989 012Labeling  
12/28/1987 011Chemistry  
7/12/1982 009Chemistry  
12/20/1973 000Approval  
 
Therapeutic Equivalents
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