Visitor Monitoring Drug History: RANITIDINE
 
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: RANITIDINE
FDA Application No: (ANDA) 075296
Active Ingredient(s): RANITIDINE HYDROCHLORIDE
Company: IVAX PHARMS
 
Label History
 
Labels are not available on this site for RANITIDINE, (ANDA) 075296
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/20/2002 007Labeling  
10/18/2001 006Facility Addition  
9/7/2000 005Packager Addition  
9/7/2000 004Facility Addition  
7/26/2000 003Labeling  
7/26/2000 002Packaging Addition  
7/26/2000 001Facility Addition  
1/14/2000 000Approval Letter 
1/28/1999 000Tentative Approval Letter 
 
Therapeutic Equivalents
©2019 Drugs That Causes a False Positive on a Drug Test