Visitor Monitoring Drug History: IMODIUM
 
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
FDA Application No: (NDA) 017690
Active Ingredient(s): LOPERAMIDE HYDROCHLORIDE
Company: MCNEIL PED
 
Label History
 
Labels are not available on this site for IMODIUM, (NDA) 017690
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/24/1993 004Manufacturing Change or Addition  
10/2/1992 003Control Supplement  
6/17/1999 002Control Supplement  
4/27/1988 001Labeling Revision  
12/28/1976 000Approval  
 
Therapeutic Equivalents
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