Visitor Monitoring Drug History: RANITIDINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: RANITIDINE HYDROCHLORIDE
FDA Application No: (ANDA) 074467
Active Ingredient(s): RANITIDINE HYDROCHLORIDE
Company: SANDOZ
 
Label History
 
Labels are not available on this site for RANITIDINE HYDROCHLORIDE, (ANDA) 074467
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/5/2002 025Control Supplement  
4/19/2002 023Control Supplement  
2/27/2001 022Control Supplement  
11/30/2000 021Packaging Addition  
11/30/2000 020Labeling  
11/30/2000 019Packager Addition  
12/7/2000 018Control Supplement  
12/7/2000 017Control Supplement  
5/25/2000 016Labeling  
3/8/2000 015Labeling  
11/9/2000 014Package Change  
6/18/1999 011Chemistry  
8/18/1999 009Chemistry  
8/18/1999 008Chemistry  
8/18/1999 007Chemistry  
8/18/1999 006Chemistry  
4/23/1999 005Labeling  
4/23/1999 004Chemistry  
12/8/1998 003Chemistry  
2/17/1998 002Chemistry  
2/17/1998 001Chemistry  
8/29/1997 000Approval Review
Review 
1/31/1996 000Tentative Approval Review
Review 
8/29/1977 000Approval Review
Review 
 
Therapeutic Equivalents
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