FDA.reportPublic FDA data

Application 210371

Type
ANDA
Sponsor
ABHAI LLC

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001DESMOPRESSIN ACETATEDESMOPRESSIN ACETATETABLET;ORAL0.1MGNoNo
002DESMOPRESSIN ACETATEDESMOPRESSIN ACETATETABLET;ORAL0.2MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
10702-169Desmopressin AcetateDesmopressin AcetateKVK-TECH, INC.ANDACurrent
10702-169Desmopressin AcetateDesmopressin AcetateKVK-TECH, INC.ANDACurrent
10702-170Desmopressin AcetateDesmopressin AcetateKVK-TECH, INC.ANDACurrent
10702-170Desmopressin AcetateDesmopressin AcetateKVK-TECH, INC.ANDACurrent