FDA.reportPublic FDA data

Application 202599

Type
ANDA
Sponsor
AUROBINDO PHARMA LTD

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001ONDANSETRON HYDROCHLORIDEONDANSETRON HYDROCHLORIDEINJECTABLE;INJECTIONEQ 2MG BASE/MLNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
55150-126OndansetronOndansetron HydrochlorideAuroMedics Pharma LLCANDACurrent
55150-126OndansetronOndansetron HydrochlorideAuroMedics Pharma LLCANDACurrent
55150-126OndansetronOndansetron HydrochlorideAuroMedics Pharma LLCANDACurrent