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Desipramine Hydrochloride - 0781-1972-01 - (Desipramine Hydrochloride)

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Drug Information of Desipramine Hydrochloride

Product NDC: 0781-1972
Proprietary Name: Desipramine Hydrochloride
Non Proprietary Name: Desipramine Hydrochloride
Active Ingredient(s): 25    mg/1 & nbsp;   Desipramine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Desipramine Hydrochloride

Product NDC: 0781-1972
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072100
Marketing Category: ANDA
Start Marketing Date: 19880524

Package Information of Desipramine Hydrochloride

Package NDC: 0781-1972-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0781-1972-01)

NDC Information of Desipramine Hydrochloride

NDC Code 0781-1972-01
Proprietary Name Desipramine Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0781-1972-01)
Product NDC 0781-1972
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desipramine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19880524
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name DESIPRAMINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Desipramine Hydrochloride


General Information