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Desipramine Hydrochloride - 52152-341-04 - (Desipramine Hydrochloride)

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Drug Information of Desipramine Hydrochloride

Product NDC: 52152-341
Proprietary Name: Desipramine Hydrochloride
Non Proprietary Name: Desipramine Hydrochloride
Active Ingredient(s): 10    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: 52152-341
Labeler Name: Actavis Totowa LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074430
Marketing Category: ANDA
Start Marketing Date: 20060509

Package Information of Desipramine Hydrochloride

Package NDC: 52152-341-04
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (52152-341-04)

NDC Information of Desipramine Hydrochloride

NDC Code 52152-341-04
Proprietary Name Desipramine Hydrochloride
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (52152-341-04)
Product NDC 52152-341
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desipramine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060509
Marketing Category Name ANDA
Labeler Name Actavis Totowa LLC
Substance Name DESIPRAMINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Desipramine Hydrochloride


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