FDA.reportPublic FDA data

Application 072099

Type
ANDA
Sponsor
SANDOZ

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001DESIPRAMINE HYDROCHLORIDEDESIPRAMINE HYDROCHLORIDETABLET;ORAL10MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0781-1971Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-1971Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-5218Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-5218Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-5218Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8218Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8218Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8218Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8218Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8218Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
68151-2482Desipramine HydrochlorideDesipramine HydrochlorideCarilion Materials ManagementANDACurrent
72189-104DESIPRAMINE HYDROCHLORIDEDESIPRAMINE HYDROCHLORIDEDIRECT RXANDACurrent