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Last Updated: December 15, 2025

Details for New Drug Application (NDA): 020070

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NDA 020070 describes COGNEX, which is a drug marketed by Shionogi Inc and is included in one NDA. Additional details are available on the COGNEX profile page.

The generic ingredient in COGNEX is tacrine hydrochloride. There are two drug master file entries for this compound. Additional details are available on the tacrine hydrochloride profile page.

Summary for 020070

Tradename:	COGNEX
Applicant:	Shionogi Inc
Ingredient:	tacrine hydrochloride
Patents:	0

Medical Subject Heading (MeSH) Categories for 020070

Cholinesterase Inhibitors
Nootropic Agents
Parasympathomimetics

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	CAPSULE;ORAL			Strength	EQ 10MG BASE
Approval Date:	Sep 9, 1993	TE:		RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	DISCN	Dosage:	CAPSULE;ORAL			Strength	EQ 20MG BASE
Approval Date:	Sep 9, 1993	TE:		RLD:	No

Profile for product number 003

Active Rx/OTC/Discontinued:	DISCN	Dosage:	CAPSULE;ORAL			Strength	EQ 30MG BASE
Approval Date:	Sep 9, 1993	TE:		RLD:	No

Expired US Patents for NDA 020070

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Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	Patent No.	Patent Expiration
Shionogi Inc	COGNEX	tacrine hydrochloride	CAPSULE;ORAL	020070-003	Sep 9, 1993	4,631,286	⤷ Get Started Free
Shionogi Inc	COGNEX	tacrine hydrochloride	CAPSULE;ORAL	020070-001	Sep 9, 1993	4,631,286	⤷ Get Started Free
Shionogi Inc	COGNEX	tacrine hydrochloride	CAPSULE;ORAL	020070-004	Sep 9, 1993	4,631,286	⤷ Get Started Free
Shionogi Inc	COGNEX	tacrine hydrochloride	CAPSULE;ORAL	020070-003	Sep 9, 1993	4,816,456	⤷ Get Started Free
Shionogi Inc	COGNEX	tacrine hydrochloride	CAPSULE;ORAL	020070-002	Sep 9, 1993	4,816,456	⤷ Get Started Free
Shionogi Inc	COGNEX	tacrine hydrochloride	CAPSULE;ORAL	020070-002	Sep 9, 1993	4,631,286	⤷ Get Started Free
Shionogi Inc	COGNEX	tacrine hydrochloride	CAPSULE;ORAL	020070-001	Sep 9, 1993	4,816,456	⤷ Get Started Free
>Applicant	>Tradename	>Generic Name	>Dosage	>NDA	>Approval Date	>Patent No.	>Patent Expiration

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