Visitor Monitoring Drug History: RANITIDINE
 
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: RANITIDINE
FDA Application No: (ANDA) 075132
Active Ingredient(s): RANITIDINE HYDROCHLORIDE
Company: RANBAXY
 
Label History
 
Labels are not available on this site for RANITIDINE, (ANDA) 075132
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/3/2002 012Control Supplement  
5/20/2002 010Package Change  
4/4/2001 009Control Supplement  
11/28/2000 008Facility Addition  
11/28/2000 007Facility Addition  
11/28/2000 006Facility Addition  
6/29/2000 005Labeling  
6/29/2000 004Facility Addition  
6/29/2000 003Formulation Revision  
6/29/2000 002Packaging Addition  
6/29/2000 001Packager Addition  
1/14/2000 000Approval Letter 
8/24/1998 000Tentative Approval Letter 
8/11/1999 000Tentative Approval Letter 
 
Therapeutic Equivalents
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