FDA.reportPublic FDA data

Application 040081

Type
ANDA
Sponsor
TEVA PHARMS

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001HYDROXYCHLOROQUINE SULFATEHYDROXYCHLOROQUINE SULFATETABLET;ORAL200MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0093-2401Hydroxychloroquine SulfateHydroxychloroquine SulfateTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-2401Hydroxychloroquine SulfateHydroxychloroquine SulfateTeva Pharmaceuticals USA, Inc.ANDACurrent
0093-2401Hydroxychloroquine SulfateHydroxychloroquine SulfateTeva Pharmaceuticals USA, Inc.ANDACurrent
0615-8374Hydroxychloroquine SulfateHydroxychloroquine SulfateNCS HealthCare of KY, Inc dba Vangard LabsANDACurrent
0615-8374Hydroxychloroquine SulfateHydroxychloroquine SulfateNCS HealthCare of KY, LLC dba Vangard LabsANDACurrent
71335-1771Hydroxychloroquine SulfateHydroxychloroquine SulfateBryant Ranch PrepackANDACurrent
71335-1771Hydroxychloroquine SulfateHydroxychloroquine SulfateBryant Ranch PrepackANDACurrent
71335-1771Hydroxychloroquine SulfateHydroxychloroquine SulfateBryant Ranch PrepackANDACurrent