Application 213496

Type
ANDA
Sponsor
SUNSHINE

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001TADALAFILTADALAFILTABLET;ORAL20MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
48792-7915TADALAFILtadalafilSunshine Lake Pharma Co., Ltd.ANDACurrent