Overview
A carbonic anhydrase inhibitor that is used as a diuretic and in the treatment of glaucoma.
Indication
For treatment of chronic open-angle glaucoma and acute angle-closure glaucoma
Associated Conditions
- Acute angle-closure glaucoma
- Open Angle Glaucoma (OAG)
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2024/03/15 | Phase 2 | Withdrawn | |||
2022/10/12 | Phase 4 | Completed | |||
2022/08/11 | Phase 4 | Active, not recruiting | |||
2016/05/03 | Phase 4 | Completed | |||
2016/05/02 | Phase 4 | Completed | |||
2015/06/04 | Phase 4 | Completed | |||
2015/03/17 | Phase 3 | Completed | |||
2012/10/05 | Phase 1 | Completed | |||
2012/04/27 | Phase 1 | Completed | |||
2005/11/23 | Phase 2 | Withdrawn |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Padagis US LLC | 0574-0791 | ORAL | 50 mg in 1 1 | 12/10/2021 | |
Effcon Laboratories, Inc. | 55806-021 | ORAL | 25 mg in 1 1 | 1/9/2024 | |
ANI Pharmaceuticals, Inc. | 62559-240 | ORAL | 25 mg in 1 1 | 5/12/2017 | |
A-S Medication Solutions | 50090-3233 | ORAL | 50 mg in 1 1 | 11/12/2018 | |
Bryant Ranch Prepack | 63629-1987 | ORAL | 50 mg in 1 1 | 5/12/2017 | |
TAGI Pharma, Inc. | 51224-124 | ORAL | 50 mg in 1 1 | 3/23/2023 | |
Bryant Ranch Prepack | 63629-1986 | ORAL | 25 mg in 1 1 | 5/12/2017 | |
Effcon Laboratories, Inc. | 55806-020 | ORAL | 50 mg in 1 1 | 1/9/2024 | |
Bryant Ranch Prepack | 72162-1754 | ORAL | 25 mg in 1 1 | 5/12/2017 | |
Padagis US LLC | 0574-0790 | ORAL | 25 mg in 1 1 | 12/10/2021 |
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 |
---|---|---|---|---|---|
No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
No TGA approvals found for this drug. |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
NEPTAZANE TABLETS 25MG | wyeth-ayerst canada inc. | 02238070 | Tablet - Oral | 25 MG | 7/24/1998 |
NEPTAZANE TABLETS 50MG | wyeth-ayerst canada inc. | 02238071 | Tablet - Oral | 50 MG | 12/23/1998 |
METHAZOLAMIDE | aa pharma inc | 02245882 | Tablet - Oral | 50 MG | 7/25/2002 |
NEPTAZANE TABLETS 25MG USP | storz, division of wyeth-ayerst canada inc. | 02019604 | Tablet - Oral | 25 MG | 12/31/1995 |
NEPTAZANE TABLETS 50MG | storz, division of wyeth-ayerst canada inc. | 02022389 | Tablet - Oral | 50 MG | 12/31/1993 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
---|---|---|---|---|---|
No CIMA AEMPS (Spain) approvals found for this drug. |
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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