Visitor Monitoring Drug History: RANITIDINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: RANITIDINE HYDROCHLORIDE
FDA Application No: (ANDA) 074864
Active Ingredient(s): RANITIDINE HYDROCHLORIDE
Company: WATSON LABS
 
Label History
 
Labels are not available on this site for RANITIDINE HYDROCHLORIDE, (ANDA) 074864
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/6/2002 005Labeling  
11/3/1999 004Chemistry  
11/3/1999 003Chemistry  
11/3/1999 002Chemistry  
8/3/1998 001Chemistry  
10/20/1997 000Approval  
7/24/1997 000Tentative Approval  
 
Therapeutic Equivalents
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