Visitor Monitoring Drug History: SKELID
 
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: SKELID
FDA Application No: (NDA) 020707
Active Ingredient(s): TILUDRONATE DISODIUM
Company: SANOFI AVENTIS US
 
Label History
 
View the label approved on November 22, 2006 for SKELID, (NDA) 020707


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
11/17/2006 005Labeling Revision Letter
Label 
8/21/2003 004Labeling Revision Letter 
6/3/1998 001Package Change  
3/7/1997 000Approval  
 
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