FDA.reportPublic FDA data

Application 087059

Type
ANDA
Sponsor
OXFORD PHARMS

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001HYDROCHLOROTHIAZIDEHYDROCHLOROTHIAZIDETABLET;ORAL25MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
50090-6157HydrochlorothiazideHydrochlorothiazideA-S Medication SolutionsANDACurrent
50090-6158HydrochlorothiazideHydrochlorothiazideA-S Medication SolutionsANDACurrent
64205-820HydrochlorothiazideHydrochlorothiazideReadyMedsANDACurrent
68788-8126HydrochlorothiazideHydrochlorothiazidePreferred Pharmaceuticals Inc.ANDACurrent
68788-8126HydrochlorothiazideHydrochlorothiazidePreferred Pharmaceuticals Inc.ANDACurrent
69584-361HydrochlorothiazideHydrochlorothiazideOxford Pharmaceuticals, LLCANDACurrent
72789-296HydrochlorothiazideHydrochlorothiazidePD-Rx Pharmaceuticals, Inc.ANDACurrent