FDA.reportPublic FDA data

Application 205675

Type
ANDA
Sponsor
AUROBINDO PHARMA LTD

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001PANTOPRAZOLE SODIUMPANTOPRAZOLE SODIUMINJECTABLE;IV (INFUSION)EQ 40MG BASE/VIALNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
55150-202Pantoprazole SodiumPantoprazole SodiumAuroMedics Pharma LLCANDACurrent
55150-202Pantoprazole SodiumPantoprazole SodiumAuroMedics Pharma LLCANDACurrent
55150-202Pantoprazole SodiumPantoprazole SodiumAuroMedics Pharma LLCANDACurrent
55150-202Pantoprazole SodiumPantoprazole SodiumAuroMedics Pharma LLCANDACurrent
55150-202Pantoprazole SodiumPantoprazole SodiumAuroMedics Pharma LLCANDACurrent
55150-202Pantoprazole SodiumPantoprazole SodiumAuroMedics Pharma LLCANDACurrent
55150-202Pantoprazole SodiumPantoprazole SodiumAuroMedics Pharma LLCANDACurrent
55154-8336Pantoprazole SodiumPantoprazole SodiumCardinal HealthANDACurrent
55154-8336Pantoprazole SodiumPantoprazole SodiumCardinal Health 107, LLCANDACurrent
55154-8336Pantoprazole SodiumPantoprazole SodiumCardinal HealthANDACurrent
55154-8336Pantoprazole SodiumPantoprazole SodiumCardinal HealthANDACurrent