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Last Updated: December 22, 2024

Details for New Drug Application (NDA): 071766


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NDA 071766 describes DESIPRAMINE HYDROCHLORIDE, which is a drug marketed by Actavis Totowa, Alembic, Amneal Pharms Co, Ani Pharms, Chartwell Rx, Heritage, Novast Labs, and Usl Pharma, and is included in sixteen NDAs. It is available from nine 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. Ten suppliers are listed for this compound. Additional details are available on the desipramine hydrochloride profile page.
Summary for 071766
Tradename:DESIPRAMINE HYDROCHLORIDE
Applicant:Actavis Totowa
Ingredient:desipramine hydrochloride
Patents:0
Pharmacology for NDA: 071766
Medical Subject Heading (MeSH) Categories for 071766
Suppliers and Packaging for NDA: 071766
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
DESIPRAMINE HYDROCHLORIDE desipramine hydrochloride TABLET;ORAL 071766 ANDA Actavis Pharma, Inc. 45963-345 45963-345-02 100 TABLET, FILM COATED in 1 BOTTLE (45963-345-02)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength100MG
Approval Date:Oct 5, 1987TE:ABRLD:No

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