FDA.reportPublic FDA data

Application 208094

Type
ANDA
Sponsor
ACTAVIS ELIZABETH

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001ALBENDAZOLEALBENDAZOLETABLET;ORAL200MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0591-2712AlbendazoleAlbendazoleActavis Pharma, Inc.ANDACurrent
0591-2712AlbendazoleAlbendazoleActavis Pharma, Inc.ANDACurrent
0591-2712AlbendazoleAlbendazoleActavis Pharma, Inc.ANDACurrent
0591-2712AlbendazoleAlbendazoleActavis Pharma, Inc.ANDACurrent