Last Updated: November 9, 2026

Details for New Drug Application (NDA): 077141

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NDA 077141 describes CITALOPRAM HYDROBROMIDE, which is a drug marketed by Almatica, Aurobindo Pharma Ltd, Pharmobedient, Aurobindo Pharma, Chartwell Molecular, Hetero Labs Ltd Iii, Hikma, Pharm Assoc, Biovail Labs Intl, Amneal Pharms Ny, Apotex, Aurobindo, Chartwell Rx, Cosette Pharms Nc, Dr Reddys Labs Ltd, Epic Pharma, Epic Pharma Llc, Fosun Pharma, Glenmark Pharms Ltd, Heritage Pharma, Invagen Pharms, Jubilant Generics, Mylan, Natco Pharma Ltd, Roxane, Sun Pharm Inds Inc, Sun Pharm Industries, Taro, and Torrent Pharms, and is included in thirty-five NDAs. It is available from thirty-six suppliers. Additional details are available on the CITALOPRAM HYDROBROMIDE profile page.

The generic ingredient in CITALOPRAM HYDROBROMIDE is citalopram hydrobromide. There is one drug master file entry for this compound. Thirty-seven suppliers are listed for this compound. Additional details are available on the citalopram hydrobromide profile page.

Summary for 077141

Tradename:	CITALOPRAM HYDROBROMIDE
Applicant:	Natco Pharma Ltd
Ingredient:	citalopram hydrobromide
Patents:	0

Medical Subject Heading (MeSH) Categories for 077141

Antidepressive Agents, Second-Generation
Serotonin Uptake Inhibitors

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	EQ 40MG BASE
Approval Date:	Apr 10, 2008	TE:		RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	EQ 20MG BASE
Approval Date:	Apr 10, 2008	TE:		RLD:	No

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