Last Updated: November 5, 2026

ATOMOXETINE Drug Patent Profile


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When do Atomoxetine patents expire, and what generic alternatives are available?

Atomoxetine is a drug marketed by Apotex, Aurobindo Pharma, Creekwood Pharms, Dr Reddys, Glenmark Pharms Ltd, Hetero Labs Ltd V, Strides Pharma, Teva Pharms Usa, and Zydus Pharms Usa Inc. and is included in nine NDAs.

The generic ingredient in ATOMOXETINE is atomoxetine hydrochloride. There is one drug master file entry for this compound. Twenty-three suppliers are listed for this compound. Additional details are available on the atomoxetine hydrochloride profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Atomoxetine

A generic version of ATOMOXETINE was approved as atomoxetine hydrochloride by ZYDUS PHARMS USA INC on September 16th, 2010.

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Summary for ATOMOXETINE
US Patents:0
Applicants:9
NDAs:9
Drug Prices: Drug price information for ATOMOXETINE
What excipients (inactive ingredients) are in ATOMOXETINE?ATOMOXETINE excipients list
DailyMed Link:ATOMOXETINE at DailyMed

US Patents and Regulatory Information for ATOMOXETINE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Hetero Labs Ltd V ATOMOXETINE HYDROCHLORIDE atomoxetine hydrochloride CAPSULE;ORAL 202682-006 Mar 11, 2021 AB RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Glenmark Pharms Ltd ATOMOXETINE HYDROCHLORIDE atomoxetine hydrochloride CAPSULE;ORAL 079019-004 May 30, 2017 AB RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Strides Pharma ATOMOXETINE HYDROCHLORIDE atomoxetine hydrochloride CAPSULE;ORAL 079021-007 Feb 18, 2021 AB RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Zydus Pharms Usa Inc ATOMOXETINE HYDROCHLORIDE atomoxetine hydrochloride CAPSULE;ORAL 079017-003 Sep 16, 2010 AB RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Strides Pharma ATOMOXETINE HYDROCHLORIDE atomoxetine hydrochloride CAPSULE;ORAL 079021-003 Feb 18, 2021 AB RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

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