MedPath

Glucosamine

Generic Name
Glucosamine
Drug Type
Small Molecule
Chemical Formula
C6H13NO5
CAS Number
3416-24-8
Unique Ingredient Identifier
N08U5BOQ1K

Overview

Osteoarthritis (OA) is a progressive and degenerative joint disease marked by loss of cartilage, bone changes, and synovial membrane inflammation. Treatment with chondroprotective drugs, such as glucosamine sulfate may offer additional benefits to nonsteroidal anti-inflammatory drugs treating the painful symptoms of OA. Glucosamine is commonly used over the counter as a treatment for arthritic joint pain, although its acceptance as a medical therapy varies due to contradictory and findings with unclear clinical significance during clinical trials. It is currently not approved as a prescription product by the FDA, but is widely available over the counter.

Indication

Glucosamine is generally used over the counter in the symptomatic treatment of osteoarthritis and joint pain, frequently combined with chondroitin sulfate and/or ibuprofen.

Associated Conditions

  • Back pain
  • Joint Pain
  • Osteoarthritis (OA)
  • Osteoarthritis of the Knee
  • Articular inflammation

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2025/08/11
Not Applicable
Completed
2024/01/11
Phase 2
Completed
2022/02/14
N/A
Completed
2022/01/28
Not Applicable
Recruiting
2019/05/03
Phase 3
Withdrawn
Eurofarma Laboratorios S.A.
2019/04/11
N/A
Completed
2018/11/16
Phase 4
Completed
2018/10/23
Phase 2
Completed
2017/06/28
N/A
UNKNOWN
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
2016/08/08
Phase 4
Completed

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Home Aide Diagnostics, Inc.
69379-285
TOPICAL
5 g in 100 g
3/9/2015
Bispit Canada Ltd.
85631-003
ORAL
130 mg in 1.3 g
8/2/2025

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
GLUCOSAMINE POWDER FOR ORAL SOLUTION 1.5G/SACHET
N/A
N/A
N/A
3/23/2009

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
No Health Canada approvals found for this drug.

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
DUARTRON 625 mg CAPSULAS DURAS
Laboratorio Reig Jofre, S.A.
75658
CÁPSULA DURA
Medicamento Sujeto A Prescripción Médica
Commercialized

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

Help Us Improve

Your feedback helps us provide better drug information and insights.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.