Visitor Monitoring Drug Details: RANITIDINE HYDROCHLORIDE
 
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Drug Details

Drug Name: RANITIDINE HYDROCHLORIDE
FDA Application No: (ANDA) 075564
Active Ingredient(s): RANITIDINE HYDROCHLORIDE
Company: GENPHARM
Original Approval or Tentative Approval Date: October 27, 2000
 
Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
RANITIDINE HYDROCHLORIDE RANITIDINE HYDROCHLORIDEEQ 150MG BASECAPSULE; ORAL Discontinued No None
RANITIDINE HYDROCHLORIDE RANITIDINE HYDROCHLORIDEEQ 300MG BASECAPSULE; ORAL Discontinued No None


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