FDA Drug Application (077050) for ONDANSETRON HYDROCHLORIDE by SUN PHARM INDS (IN)

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Application Number077050
Product Number001
FormTABLET;ORAL
DosageEQ 4MG BASE
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameONDANSETRON HYDROCHLORIDE
Active IngredientONDANSETRON HYDROCHLORIDE

Active IngredientCount
List of drugs with Active Ingredient ONDANSETRON HYDROCHLORIDE6


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