Application 087197

Type
ANDA
Sponsor
WATSON LABS

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001SULFASALAZINESULFASALAZINETABLET;ORAL500MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
68788-9021SULFASALAZINESULFASALAZINEPreferred PharmaceuticalsANDACurrent
68788-9021SULFASALAZINESULFASALAZINEPreferred Pharmaceuticals, IncANDACurrent