FDA.reportPublic FDA data

Application 072100

Type
ANDA
Sponsor
SANDOZ

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
0781-1972Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-1972Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-1972Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8972Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8972Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8972Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8972Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
0781-8972Desipramine HydrochlorideDesipramine HydrochlorideSandoz IncANDACurrent
21695-428Desipramine HydrochlorideDesipramine HydrochlorideRebel Distributors CorpANDACurrent
68084-972Desipramine HydrochlorideDesipramine HydrochlorideAmerican Health PackagingANDACurrent