FDA.reportPublic FDA data

Application 071601

Type
ANDA
Sponsor
ACTAVIS TOTOWA

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001DESIPRAMINE HYDROCHLORIDEDESIPRAMINE HYDROCHLORIDETABLET;ORAL25MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
45963-342Desipramine HydrochlorideDesipramine HydrochlorideActavis Pharma, Inc.ANDACurrent
45963-342Desipramine HydrochlorideDesipramine HydrochlorideActavis Pharma, Inc.ANDACurrent