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) 019488
Active Ingredient(s): NICARDIPINE HYDROCHLORIDE
Company: PDL BIOPHARMA INC
 
Label History
 
Labels are not available on this site for CARDENE, (NDA) 019488
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/9/2001 009Package Change  
9/20/1999 008Labeling Revision  
12/30/1994 007Manufacturing Change or Addition  
12/17/1992 006Formulation Revision  
10/16/1990 005Control Supplement  
6/7/1990 004Package Change  
9/12/1989 003Package Change  
9/12/1989 002Control Supplement  
4/18/1989 001Control Supplement  
12/21/1988 000Approval  
 
Therapeutic Equivalents
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