Visitor Monitoring Drug History: IMODIUM A-D
 
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 A-D
FDA Application No: (NDA) 019860
Active Ingredient(s): LOPERAMIDE HYDROCHLORIDE
Company: MCNEIL CONS
 
Label History
 
Labels are not available on this site for IMODIUM AD, (NDA) 019860
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/16/2004 020Labeling Revision Letter 
9/26/2000 019Manufacturing Change or Addition  
4/5/2001 018Labeling Revision Letter 
5/11/2000 017Manufacturing Change or Addition  
11/29/1999 016Manufacturing Change or Addition  
11/24/1999 015Manufacturing Change or Addition  
9/4/1998 013Package Change  
2/6/1997 012Manufacturing Change or Addition  
1/3/1994 011Manufacturing Change or Addition  
8/15/1994 010Labeling Revision  
2/2/1995 009Package Change  
2/2/1995 008Control Supplement  
2/2/1995 007Manufacturing Change or Addition  
3/22/1995 006Formulation Revision  
7/6/1993 005Manufacturing Change or Addition  
11/23/1992 004Labeling Revision  
1/6/1992 002Manufacturing Change or Addition  
7/25/1991 001Labeling Revision  
11/22/1989 000Approval  
 
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