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2019/05/03 | Phase 3 | Withdrawn | Eurofarma Laboratorios S.A. | ||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 |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
Quality Health Australia Daily Glucosamine Sulfate 1500mg | 235126 | Pharmacare Laboratories Pty Ltd | Medicine | A | 3/17/2015 |
Glucosamine HCL 1500mg TAB | 169608 | Medicine | A | 3/5/2010 | |
Glucosamine Powder Sachet | 157319 | Medicine | A | 11/27/2008 | |
JointBiotics Glucosamine 1500mg and Chondroitin 100mg | 302975 | Medicine | A | 5/14/2018 | |
YHL 3 IN 1 FORMULA JOINT MOBILITY | 354030 | Medicine | A | 2/2/2021 | |
Glucosamine Premium Repair | 315815 | Medicine | A | 3/27/2019 | |
Austar Joint Care | 444208 | Medicine | A | 3/22/2024 | |
JoinTQ | 384091 | Medicine | A | 2/16/2022 | |
BioSource Glucosamine HCl 1500 mg | 331183 | Medicine | A | 3/16/2020 | |
Thompson's Glucosamine & Chondroitin with Boron | 406330 | Medicine | A | 3/17/2023 |
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. |
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