Visitor Monitoring Drug History: CARDENE
 
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: CARDENE
FDA Application No: (NDA) 019734
Active Ingredient(s): NICARDIPINE HYDROCHLORIDE
Company: PDL BIOPHARMA INC
 
Label History
 
Labels are not available on this site for CARDENE, (NDA) 019734
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/22/2007 009Labeling Revision Letter 
10/24/2002 005Control Supplement  
4/29/1997 004Manufacturing Change or Addition  
4/10/1995 003Control Supplement  
5/12/1995 002Manufacturing Change or Addition  
11/20/1992 001Control Supplement  
1/30/1992 000Approval  
 
There are no Therapeutic Equivalents
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