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Generated: April 26, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 071602

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NDA 071602 describes DESIPRAMINE HYDROCHLORIDE, which is a drug marketed by Actavis Totowa, Amneal Pharms Co, Ani Pharms Inc, Heritage Pharms Inc, Ingenus Pharms Llc, Mountain, Sandoz, and Usl Pharma, and is included in twenty NDAs. It is available from thirteen suppliers. Additional details are available on the DESIPRAMINE HYDROCHLORIDE profile page.

The generic ingredient in DESIPRAMINE HYDROCHLORIDE is desipramine hydrochloride. There are nine drug master file entries for this compound. Sixteen suppliers are listed for this compound. Additional details are available on the desipramine hydrochloride profile page.
Summary for 071602
Tradename:DESIPRAMINE HYDROCHLORIDE
Applicant:Actavis Totowa
Ingredient:desipramine hydrochloride
Patents:0
Therapeutic Class:Antidepressants
Formulation / Manufacturing:see details
Pharmacology for NDA: 071602
Medical Subject Heading (MeSH) Categories for 071602
Suppliers and Packaging for NDA: 071602
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
DESIPRAMINE HYDROCHLORIDE desipramine hydrochloride TABLET;ORAL 071602 ANDA Actavis Pharma, Inc. 45963-344 N 45963-344-02

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength75MG
Approval Date:Oct 5, 1987TE:ABRLD:No

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