Visitor Monitoring Drug History: PARAPLATIN
 
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: PARAPLATIN
FDA Application No: (NDA) 020452
Active Ingredient(s): CARBOPLATIN
Company: BRISTOL MYERS SQUIBB
 
Label History
 
View the label approved on January 15, 2004 for PARAPLATIN, (NDA) 020452


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
1/9/2004 001Control Supplement Letter
Label 
7/14/2003 000Approval Letter
Label
Review 
 
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