Visitor Monitoring Drug History: RANITIDINE
 
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Label and Approval History

Drug Name: RANITIDINE
FDA Application No: (ANDA) 075094
Active Ingredient(s): RANITIDINE HYDROCHLORIDE
Company: LEINER
 
Label History
 
Labels are not available on this site for RANITIDINE, (ANDA) 075094
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/21/2000 009Facility Addition  
1/6/2000 001Package Change  
6/21/1999 000Approval Letter 
1/26/1999 000Tentative Approval Letter 
 
Therapeutic Equivalents
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