FDA.reportPublic FDA data

Application 072693

Type
ANDA
Sponsor
BARR

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001NORTREL 1/35-21ETHINYL ESTRADIOL; NORETHINDRONETABLET;ORAL-210.035MG;1MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0555-9009NortrelNorethindrone and Ethinyl EstradiolTeva Pharmaceuticals USA, Inc.ANDACurrent
0555-9009NortrelNorethindrone and Ethinyl EstradiolTeva Pharmaceuticals USA, Inc.ANDACurrent
0555-9009NortrelNorethindrone and Ethinyl EstradiolTeva Pharmaceuticals USA, Inc.ANDACurrent
0555-9009NortrelNorethindrone and Ethinyl EstradiolTeva Pharmaceuticals USA, Inc.ANDACurrent
0555-9009NortrelNorethindrone and Ethinyl EstradiolTeva Pharmaceuticals USA, Inc.ANDACurrent
0555-9009NortrelNorethindrone and Ethinyl EstradiolTeva Pharmaceuticals USA, Inc.ANDACurrent