FDA.reportPublic FDA data

Application 211556

Type
ANDA
Sponsor
EYWA PHARMA

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001ACETAZOLAMIDEACETAZOLAMIDETABLET;ORAL125MGNoNo
002ACETAZOLAMIDEACETAZOLAMIDETABLET;ORAL250MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
50090-5217AcetazolamideAcetazolamideA-S Medication SolutionsANDACurrent
60687-619AcetazolamideAcetazolamideAmerican Health PackagingANDACurrent
60687-619AcetazolamideAcetazolamideAmerican Health PackagingANDACurrent
70934-926AcetazolamideAcetazolamideDenton Pharma, Inc. DBA Northwind PharmaceuticalsANDACurrent
70934-926AcetazolamideAcetazolamideDenton Pharma, Inc. DBA Northwind PharmaceuticalsANDACurrent
71930-008AcetazolamideAcetazolamideEywa Pharma IncANDACurrent
71930-008AcetazolamideAcetazolamideEywa Pharma IncANDACurrent
71930-008AcetazolamideAcetazolamideEywa Pharma IncANDACurrent
71930-009AcetazolamideAcetazolamideEywa Pharma IncANDACurrent
71930-009AcetazolamideAcetazolamideEywa Pharma IncANDACurrent
71930-009AcetazolamideAcetazolamideEywa Pharma IncANDACurrent
72789-237AcetazolamideAcetazolamidePD-Rx Pharmaceuticals, Inc.ANDACurrent
72789-237AcetazolamideAcetazolamidePD-Rx Pharmaceuticals, Inc.ANDACurrent
72789-238AcetazolamideAcetazolamidePD-Rx Pharmaceuticals, Inc.ANDACurrent
72789-238AcetazolamideAcetazolamidePD-Rx Pharmaceuticals, Inc.ANDACurrent