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Last Updated: November 2, 2024

Details for New Drug Application (NDA): 072103

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NDA 072103 describes DESIPRAMINE HYDROCHLORIDE, which is a drug marketed by Actavis Totowa, Alembic, Amneal Pharms Co, Ani Pharms, Chartwell Rx, Heritage Pharms, 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 072103

Tradename:	DESIPRAMINE HYDROCHLORIDE
Applicant:	Chartwell Rx
Ingredient:	desipramine hydrochloride
Patents:	0

Medical Subject Heading (MeSH) Categories for 072103

Adrenergic Uptake Inhibitors
Antidepressive Agents, Tricyclic
Enzyme Inhibitors

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	100MG
Approval Date:	Jun 20, 1988	TE:	AB	RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	10MG
Approval Date:	May 24, 1988	TE:	AB	RLD:	No

Profile for product number 003

Active Rx/OTC/Discontinued:	RX	Dosage:	TABLET;ORAL			Strength	25MG
Approval Date:	May 24, 1988	TE:	AB	RLD:	No

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