Last Updated: September 24, 2026

Details for New Drug Application (NDA): 078751

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NDA 078751 describes NARATRIPTAN, which is a drug marketed by Ani Pharms, Apotex Corp, Aurobindo Pharma Usa, Chartwell Rx, Heritage, Hikma, Orbion Pharms, Padagis Us, and Sun Pharm Inds Ltd, and is included in nine NDAs. It is available from four suppliers. Additional details are available on the NARATRIPTAN profile page.

The generic ingredient in NARATRIPTAN is naratriptan hydrochloride. There is one drug master file entry for this compound. Four suppliers are listed for this compound. Additional details are available on the naratriptan hydrochloride profile page.

Summary for 078751

Tradename:	NARATRIPTAN
Applicant:	Ani Pharms
Ingredient:	naratriptan hydrochloride
Patents:	0

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	EQ 1MG BASE
Approval Date:	Jul 7, 2010	TE:		RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	EQ 2.5MG BASE
Approval Date:	Jul 7, 2010	TE:		RLD:	No

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