Visitor Monitoring Drug History: CIMETIDINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: CIMETIDINE HYDROCHLORIDE
FDA Application No: (ANDA) 074757
Active Ingredient(s): CIMETIDINE HYDROCHLORIDE
Company: MORTON GROVE
 
Label History
 
Labels are not available on this site for CIMETIDINE HYDROCHLORIDE, (ANDA) 074757
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
10/17/1997 000Approval  
 
Therapeutic Equivalents
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