Visitor Monitoring Drug History: RENOVUE-DIP
 
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: RENOVUE-DIP
FDA Application No: (NDA) 017903
Active Ingredient(s): IODAMIDE MEGLUMINE
Company: BRACCO
 
Label History
 
Labels are not available on this site for RENOVUEDIP, (NDA) 017903
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/11/1995 009Labeling Revision  
3/21/1994 008Control Supplement  
7/23/1985 007Labeling Revision  
8/6/1985 006Manufacturing Change or Addition  
2/22/1983 005Expiration Date Change  
11/23/1982 004General Efficacy (MarkIV)  
1/22/1980 002Control Supplement  
7/25/1980 001Labeling Revision  
7/25/1978 000Approval  
 
There are no Therapeutic Equivalents
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