Visitor Monitoring Drug History: RANITIDINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: RANITIDINE HYDROCHLORIDE
FDA Application No: (ANDA) 074655
Active Ingredient(s): RANITIDINE HYDROCHLORIDE
Company: SANDOZ
 
Label History
 
Labels are not available on this site for RANITIDINE HYDROCHLORIDE, (ANDA) 074655
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/19/2002 011Control Supplement  
11/6/2001 010Control Supplement  
3/19/2001 009Control Supplement  
1/26/2001 008Control Supplement  
11/30/2000 007Control Supplement  
5/25/2000 006Labeling  
3/3/2000 005Labeling  
2/2/2000 004Control Supplement  
8/9/1999 003Chemistry  
5/20/1998 002Chemistry  
5/20/1998 001Chemistry  
10/22/1997 000Approval Review 
7/24/1997 000Tentative Approval Review 
 
Therapeutic Equivalents
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