FDA.reportPublic FDA data

Application 072104

Type
ANDA
Sponsor
SANDOZ

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001DESIPRAMINE HYDROCHLORIDEDESIPRAMINE HYDROCHLORIDETABLET;ORAL150MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0781-1976Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-1976Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-1976Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8976Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8976Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8976Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8976Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8976Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent