FDA.reportPublic FDA data

Application 072102

Type
ANDA
Sponsor
SANDOZ

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001DESIPRAMINE HYDROCHLORIDEDESIPRAMINE HYDROCHLORIDETABLET;ORAL75MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0781-1974Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-1974Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-1974Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8974Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8974Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8974Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8974Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8974Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent