Visitor Monitoring Drug History: ZINECARD
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
Label and Approval History

Drug Name: ZINECARD
FDA Application No: (NDA) 020212
Active Ingredient(s): DEXRAZOXANE HYDROCHLORIDE
Company: PHARMACIA AND UPJOHN
 
Label History
 
View the label approved on May 25, 2005 for ZINECARD, (NDA) 020212


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/20/2005 008Labeling Revision Letter
Label 
10/31/2002 006Accelerated Approval Letter
Label 
10/31/2002 005Labeling Revision Letter
Label 
10/31/2002 004Labeling Revision Letter
Label 
5/8/2001 003Manufacturing Change or Addition  
5/26/1995 000Approval Label 
 
Therapeutic Equivalents
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