Overview
A thiazide diuretic with actions and uses similar to those of hydrochlorothiazide. (From Martindale, The Extra Pharmacopoeia, 30th ed, p812)
Indication
Chlorothiazide is indicated as adjunctive therapy in edema associated with congestive heart failure, hepatic cirrhosis, and corticosteroid and estrogen therapy. It is also indicated in the management of hypertension either as the sole therapeutic agent or to enhance the effectiveness of other antihypertensive drugs in the more severe forms of hypertension.
Associated Conditions
- Edema
- Hypertension
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2018/07/02 | Phase 4 | Terminated | |||
2015/11/17 | Phase 4 | Completed | |||
2015/09/11 | Phase 1 | Completed | |||
1999/10/28 | Phase 3 | Completed | |||
1999/10/19 | N/A | Completed | National Center for Research Resources (NCRR) |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Akorn | 17478-419 | INTRAVENOUS | 500 mg in 1 1 | 8/10/2012 | |
Sun Pharmaceutical Industries, Inc. | 47335-330 | INTRAVENOUS | 500 mg in 18 mL | 10/1/2019 | |
Sagent Pharmaceuticals | 25021-305 | INTRAVENOUS | 500 mg in 18 mL | 10/23/2019 | |
Akorn | 76478-711 | INTRAVENOUS | 0.5 mg in 18 mL | 6/12/2012 | |
Fresenius Kabi USA, LLC | 63323-658 | INTRAVENOUS | 500 mg in 18 mL | 7/10/2017 | |
Fresenius Kabi USA, LLC | 63323-658 | INTRAVENOUS | 500 mg in 18 mL | 5/31/2023 | |
Fresenius Kabi USA, LLC | 63323-658 | INTRAVENOUS | 500 mg in 18 mL | 6/2/2023 | |
Sagent Pharmaceuticals | 25021-305 | INTRAVENOUS | 500 mg in 18 mL | 11/16/2020 | |
American Regent, Inc. | 0517-1820 | INTRAVENOUS | 500 mg in 18 mL | 6/5/2020 | |
Salix Pharmaceuticals, Inc | 65649-311 | ORAL | 250 mg in 5 mL | 11/1/2021 |
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. |
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