Visitor Monitoring Drug History: RANITIDINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: RANITIDINE HYDROCHLORIDE
FDA Application No: (ANDA) 074023
Active Ingredient(s): RANITIDINE HYDROCHLORIDE
Company: GENPHARM
 
Label History
 
Labels are not available on this site for RANITIDINE HYDROCHLORIDE, (ANDA) 074023
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/18/2001 014Control Supplement  
9/29/2000 009Supplier Addition  
7/26/2000 008Supplier Addition  
1/6/2000 007Chemistry  
2/16/1999 006Chemistry  
8/4/1999 005Chemistry  
8/26/1998 004Labeling  
3/25/1998 003Chemistry  
3/25/1998 002Chemistry  
8/26/1998 001Chemistry  
8/22/1997 000Approval  
6/17/1997 000Tentative Approval  
 
Therapeutic Equivalents
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