FDA Drug Application (075132) for RANITIDINE HYDROCHLORIDE by SUN PHARM INDS LTD

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Application Number075132
Product Number001
FormTABLET;ORAL
DosageEQ 75MG BASE
Product Market Status Discontinued
Therapeutic Equivalence Evaluation Code
Reference Drug
Drug NameRANITIDINE HYDROCHLORIDE
Active IngredientRANITIDINE HYDROCHLORIDE

Active IngredientCount
List of drugs with Active Ingredient RANITIDINE HYDROCHLORIDE7


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