FDA.reportPublic FDA data

Application 201749

Type
ANDA
Sponsor
SUN PHARM

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001METHOTREXATE SODIUMMETHOTREXATE SODIUMTABLET;ORALEQ 2.5MG BASENoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
47335-235MethotrexateMethotrexate SodiumSun Pharmaceutical Industries, Inc.ANDACurrent
47335-235MethotrexateMethotrexate SodiumSun Pharmaceutical Industries, Inc.ANDACurrent
47335-235MethotrexateMethotrexate SodiumSun Pharmaceutical Industries, Inc.ANDACurrent
50090-3418MethotrexateMethotrexate SodiumA-S Medication SolutionsANDACurrent
50090-3418MethotrexateMethotrexate SodiumA-S Medication SolutionsANDACurrent
50090-3418MethotrexateMethotrexate SodiumA-S Medication SolutionsANDACurrent
50090-3418MethotrexateMethotrexate SodiumA-S Medication SolutionsANDACurrent
70518-1251MethotrexateMethotrexate SodiumREMEDYREPACK INC.ANDACurrent
70518-1251MethotrexateMethotrexate SodiumREMEDYREPACK INC.ANDACurrent