Visitor Monitoring Drug History: PEPCID
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
Label and Approval History

Drug Name: PEPCID
FDA Application No: (NDA) 019462
Active Ingredient(s): FAMOTIDINE
Company: MERCK
 
Label History
 
View the label approved on June 6, 2002 for PEPCID, (NDA) 019462


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/29/2002 032Control Supplement  
3/14/2001 031Labeling Revision Letter 
6/6/2002 030Efficacy Supplement with Clinical Data to Support Letter
Label
Review 
4/25/2001 029Labeling Revision Label 
11/27/2000 028Labeling Revision  
3/18/1999 027Labeling Revision Review 
10/8/1998 026Labeling Revision  
2/8/1999 025Control Supplement  
11/25/1998 024Manufacturing Change or Addition  
8/22/1997 023Labeling Revision  
8/12/1998 022Labeling Revision  
1/9/1997 021Control Supplement  
2/6/1996 020Manufacturing Change or Addition  
11/13/1996 019Package Change  
3/29/1996 018Labeling Revision  
3/17/1995 017Control Supplement  
3/29/1996 016Labeling Revision  
3/29/1996 015Labeling Revision  
11/30/1990 012Labeling Revision  
8/22/1997 011Labeling Revision  
12/10/1991 010New or Modified Indication  
11/30/1990 008Labeling Revision  
11/30/1990 007Labeling Revision  
8/16/1991 006Manufacturing Change or Addition  
11/23/1988 005Labeling Revision  
8/18/1988 004Package Change  
10/17/1988 003New or Modified Indication  
4/1/1987 002Labeling Revision  
12/12/1986 001Labeling Revision  
10/15/1986 000Approval Label 
 
©2019 Drugs That Causes a False Positive on a Drug Test