Visitor Monitoring Drug History: RANITIDINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: RANITIDINE HYDROCHLORIDE
FDA Application No: (ANDA) 074488
Active Ingredient(s): RANITIDINE HYDROCHLORIDE
Company: TEVA
 
Label History
 
Labels are not available on this site for RANITIDINE HYDROCHLORIDE, (ANDA) 074488
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
5/22/2001 018Facility Addition  
12/13/2001 016Packaging Addition  
12/13/2001 015Control Supplement  
12/13/2001 014Facility Addition  
12/13/2001 013Manufacturing Revision  
9/11/2000 012Labeling  
4/6/2000 011Labeling  
4/6/2000 010Labeling  
6/7/1999 008Chemistry  
7/14/1999 007Chemistry  
8/30/2000 006Chemistry  
8/30/2000 005Labeling  
8/30/2000 004Chemistry  
8/30/2000 003Chemistry  
6/15/1999 002Chemistry  
3/12/1999 001Chemistry  
7/31/1997 000Approval  
3/5/1996 000Tentative Approval  
 
Therapeutic Equivalents
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