FDA.reportPublic FDA data

Application 212902

Type
ANDA
Sponsor
HAVIX

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
59746-780HYDROXYCHLOROQUINE SULFATEhydroxychloroquine sulfateJubilant Cadista Pharmaceuticals Inc.ANDACurrent
59746-780HYDROXYCHLOROQUINE SULFATEhydroxychloroquine sulfateJubilant Cadista Pharmaceuticals Inc.ANDACurrent
59746-780HYDROXYCHLOROQUINE SULFATEhydroxychloroquine sulfateJubilant Cadista Pharmaceuticals Inc.ANDACurrent
63629-2425HYDROXYCHLOROQUINE SULFATEhydroxychloroquine sulfateBryant Ranch PrepackANDACurrent
71337-019HYDROXYCHLOROQUINE SULFATEhydroxychloroquine sulfateHavix Group Inc d-b-a Aavis PharmaceuticalsANDACurrent
71337-019HYDROXYCHLOROQUINE SULFATEhydroxychloroquine sulfateHavix Group Inc d-b-a Aavis PharmaceuticalsANDACurrent