FDA Drug Application (077172) for ONDANSETRON HYDROCHLORIDE by SUN PHARM INDS (IN)

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Application Number077172
Product Number001
FormINJECTABLE;INJECTION
DosageEQ 2MG BASE/ML
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AP Injectable aqueous solutions and, in certain instances, intravenous non-aqueous solutions
Reference Drug
Drug NameONDANSETRON HYDROCHLORIDE
Active IngredientONDANSETRON HYDROCHLORIDE



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