Visitor Monitoring Drug History: CIMETIDINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: CIMETIDINE HYDROCHLORIDE
FDA Application No: (ANDA) 074610
Active Ingredient(s): CIMETIDINE HYDROCHLORIDE
Company: TEVA
 
Label History
 
Labels are not available on this site for CIMETIDINE HYDROCHLORIDE, (ANDA) 074610
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
8/30/2001 006Facility Addition  
7/7/2000 005Facility Addition  
1/24/2000 004Packaging Addition  
10/28/1997 003Chemistry  
10/14/1997 002Chemistry  
4/7/1997 001Chemistry  
9/26/1996 000Approval  
 
Therapeutic Equivalents
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