Visitor Monitoring Drug History: REGLAN
 
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: REGLAN
FDA Application No: (NDA) 018821
Active Ingredient(s): METOCLOPRAMIDE HYDROCHLORIDE
Company: ROBINS AH
 
Label History
 
Labels are not available on this site for REGLAN, (NDA) 018821
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/7/2001 020Labeling Revision Letter 
3/9/1999 018Labeling Revision Review 
1/30/1998 017Manufacturing Change or Addition  
6/1/2000 016Labeling Revision  
6/24/1996 015Labeling Revision  
5/31/1994 014Labeling Revision  
2/22/1989 013Labeling Revision  
8/31/1992 012Control Supplement  
5/5/1987 010Labeling Revision  
10/21/1986 009Labeling Revision  
11/4/1986 008Package Change  
4/23/1986 007Labeling Revision  
10/21/1985 006Labeling Revision  
8/20/1985 005Labeling Revision  
3/12/1985 004Labeling Revision  
9/23/1983 003Control Supplement  
8/12/1983 002Control Supplement  
7/5/1983 001Labeling Revision  
3/25/1983 000Approval  
 
Therapeutic Equivalents
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