Visitor Monitoring Drug History: INNOHEP
 
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: INNOHEP
FDA Application No: (NDA) 020484
Active Ingredient(s): TINZAPARIN SODIUM
Company: PHARMION
 
Label History
 
View the label approved on July 14, 2000 for INNOHEP, (NDA) 020484


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
11/7/2006 006Labeling Revision Letter 
3/4/2003 003Labeling Revision Letter 
2/5/2002 002Labeling Revision Letter 
11/21/2000 001Control Supplement  
7/14/2000 000Approval Letter
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