FDA.reportPublic FDA data

Application 083745

Type
ANDA
Sponsor
SANDOZ

Application Products#

Product, Drug, Ingredient table
ProductDrugIngredientFormStrengthReference drugReference standard
001IMIPRAMINE HYDROCHLORIDEIMIPRAMINE HYDROCHLORIDETABLET;ORAL25MGNoNo

NDC Listings For This Application#

NDC, Name, Nonproprietary name table
NDCNameNonproprietary nameLabelerMarketing categoryStatus
0781-1764Imipramine HydrochlorideImipramine HydrochlorideSandoz IncANDACurrent
0781-1764Imipramine HydrochlorideImipramine HydrochlorideSandoz IncANDACurrent
0781-1764Imipramine HydrochlorideImipramine HydrochlorideSandoz IncANDACurrent
55289-144Imipramine HydrochlorideImipramine HydrochloridePD-Rx Pharmaceuticals, InANDACurrent
55289-144Imipramine HydrochlorideImipramine HydrochloridePD-Rx Pharmaceuticals, Inc.ANDACurrent
55289-144Imipramine HydrochlorideImipramine HydrochloridePD-Rx Pharmaceuticals, Inc.ANDACurrent
55289-144Imipramine HydrochlorideImipramine HydrochloridePD-Rx Pharmaceuticals, Inc.ANDACurrent
55289-144Imipramine HydrochlorideImipramine HydrochloridePD-Rx Pharmaceuticals, Inc.ANDACurrent