Visitor Monitoring Drug History: ZANTAC 75
 
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Label and Approval History

Drug Name: ZANTAC 75
FDA Application No: (NDA) 020745
Active Ingredient(s): RANITIDINE HYDROCHLORIDE
Company: BOEHRINGER INGELHEIM
 
Label History
 
Labels are not available on this site for ZANTAC 75, (NDA) 020745
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/8/1999 001New or Modified Indication  
2/26/1998 000Approval Review 
 
There are no Therapeutic Equivalents
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