TheraRadar
Data updated: Mar 29, 2026

ADLARITY

DONEPEZIL HYDROCHLORIDE
Approved 2022-03-11
1
Indication
--
Phase 3 Trials
4
Years on Market

Details

Status
Discontinued
First Approved
2022-03-11
Routes
TRANSDERMAL
Dosage Forms
SYSTEM

Companies

Active Ingredient: DONEPEZIL HYDROCHLORIDE

ADLARITY Approval History

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What ADLARITY Treats

1 FDA approvals

Originally approved for its first indication in 2022 .

  • Other (1)
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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

ADLARITY FDA Label Details

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ADLARITY Patents & Exclusivity

Latest Patent: Aug 2038

Patents (44 active)

US10966936 Expires Aug 11, 2038
US10835499 Expires May 20, 2038
US11648214 Expires Sep 23, 2037
US11103463 Expires Jul 26, 2037
US10016372 Expires Jul 26, 2037
US10300025 Expires Jul 26, 2037
US10307379 Expires Jul 26, 2037
US9993466 Expires Jul 26, 2037
US11679086 Expires May 26, 2037
US12161767 Expires Dec 30, 2036
+ 34 more patents
Source: FDA Orange Book

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.