FDA.reportPublic FDA data

Application 071891

Type
ANDA
Sponsor
WATSON LABS

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001SULINDACSULINDACTABLET;ORAL150MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0591-5661SulindacSulindacActavis Pharma, Inc.ANDACurrent
0591-5661SulindacSulindacActavis Pharma, Inc.ANDACurrent
0591-5661SulindacSulindacActavis Pharma, Inc.ANDACurrent
0591-5661SulindacSulindacActavis Pharma, Inc.ANDACurrent
0591-5661SulindacSulindacActavis Pharma, Inc.ANDACurrent