Visitor Monitoring Drug History: RANITIDINE HYDROCHLORIDE
 
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Label and Approval History

Drug Name: RANITIDINE HYDROCHLORIDE
FDA Application No: (ANDA) 075165
Active Ingredient(s): RANITIDINE HYDROCHLORIDE
Company: IVAX PHARMS
 
Label History
 
Labels are not available on this site for RANITIDINE HYDROCHLORIDE, (ANDA) 075165
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
11/23/1999 001Facility Addition  
9/30/1998 000Approval Letter 
 
Therapeutic Equivalents
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