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Last Updated: November 22, 2024

Details for New Drug Application (NDA): 071601

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NDA 071601 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 071601

Tradename:	DESIPRAMINE HYDROCHLORIDE
Applicant:	Actavis Totowa
Ingredient:	desipramine hydrochloride
Patents:	0

Pharmacology for NDA: 071601

Medical Subject Heading (MeSH) Categories for 071601

Adrenergic Uptake Inhibitors
Antidepressive Agents, Tricyclic
Enzyme Inhibitors

Suppliers and Packaging for NDA: 071601

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
DESIPRAMINE HYDROCHLORIDE	desipramine hydrochloride	TABLET;ORAL	071601	ANDA	Actavis Pharma, Inc.	45963-342	45963-342-02	100 TABLET, FILM COATED in 1 BOTTLE (45963-342-02)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	25MG
Approval Date:	Jun 5, 1987	TE:	AB	RLD:	No

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