Visitor Monitoring Drug History: IMODIUM ADVANCED
 
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: IMODIUM ADVANCED
FDA Application No: (NDA) 020606
Active Ingredient(s): LOPERAMIDE HYDROCHLORIDE; SIMETHICONE
Company: MCNEIL
 
Label History
 
Labels are not available on this site for IMODIUM ADVANCED, (NDA) 020606
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/16/2004 009Labeling Revision Letter 
6/21/2001 008Control Supplement  
11/29/1999 007Manufacturing Change or Addition  
12/3/1999 006Manufacturing Change or Addition  
10/4/1999 005Manufacturing Change or Addition  
10/14/1998 004Manufacturing Change or Addition  
9/4/1998 002Package Change  
9/10/1998 001Control Supplement  
6/26/1997 000Approval Review 
 
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