TheraRadar
Data updated: May 26, 2026

GALANTAMINE HYDROBROMIDE

CNS Approved 2008-08-28

Galantamine hydrobromide extended-release capsules are indicated for the treatment of mild to moderate dementia of the Alzheimer's type.

Source: FDA Label • Aurobindo Pharma
18
Indications
--
Phase 3 Trials
17
Years on Market

GALANTAMINE HYDROBROMIDE Approval History

2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
289 FDA actions from 2008 to 2025
Mar 2025 SUPPL
Label · Labeling
Feb 2025 SUPPL
Label · Labeling
Nov 2024 SUPPL
Label · Labeling

What GALANTAMINE HYDROBROMIDE Treats

18 FDA approvals

Originally approved for its first indication in 2008 . Covers 18 distinct patient populations.

  • Other (18)
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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.

GALANTAMINE HYDROBROMIDE FDA Label Details

Indications & Usage

FDA Label (PDF)

Galantamine hydrobromide extended-release capsules are indicated for the treatment of mild to moderate dementia of the Alzheimer's type. Galantamine hydrobromide is a cholinesterase inhibitor indicated for the treatment of mild to moderate dementia of the Alzheimer’s type

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Data Sources

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