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Desipramine Hydrochloride - 52152-345-05 - (Desipramine Hydrochloride)

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Drug Information of Desipramine Hydrochloride

Product NDC: 52152-345
Proprietary Name: Desipramine Hydrochloride
Non Proprietary Name: Desipramine Hydrochloride
Active Ingredient(s): 100    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: 52152-345
Labeler Name: Actavis Totowa LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071766
Marketing Category: ANDA
Start Marketing Date: 20060719

Package Information of Desipramine Hydrochloride

Package NDC: 52152-345-05
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (52152-345-05)

NDC Information of Desipramine Hydrochloride

NDC Code 52152-345-05
Proprietary Name Desipramine Hydrochloride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (52152-345-05)
Product NDC 52152-345
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desipramine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060719
Marketing Category Name ANDA
Labeler Name Actavis Totowa LLC
Substance Name DESIPRAMINE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Desipramine Hydrochloride


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