Visitor Monitoring Drug History: CARDIZEM
 
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: CARDIZEM
FDA Application No: (NDA) 020792
Active Ingredient(s): DILTIAZEM HYDROCHLORIDE
Company: BIOVAIL
 
Label History
 
Labels are not available on this site for CARDIZEM, (NDA) 020792
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/4/2001 004Control Supplement  
1/26/2001 003Manufacturing Change or Addition  
11/20/1997 001Control Supplement  
9/5/1997 000Approval Review 
 
Therapeutic Equivalents
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