FDA.reportPublic FDA data

Application 212913

Type
ANDA
Sponsor
MYLAN

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001SUCRALFATESUCRALFATESUSPENSION;ORAL1GM/10MLNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0378-9205sucralfatesucralfateMylan Pharmaceuticals Inc.ANDACurrent
0378-9205sucralfatesucralfateMylan Pharmaceuticals Inc.ANDACurrent