Active substance
Chlorothiazide
- SFDA 7
- US FDA 21
- WHO EML 2
SFDA Saudi Arabia — SFDA human drug list
| Trade name | Strength | Form · route | Pack | Public price | Type | Company | Status |
|---|---|---|---|---|---|---|---|
| Chlorothiazide BOS | 500 mg | powder for solution for injection · Intravenous use | 1 Vial | SAR 461.90 | Generic · Prescription | Boston Oncology Arabia | Valid |
| MICARDIS PLUS | 80,12.5 mg,mg | Tablet · Oral use | 28 Blister | SAR 65.05 | NCE · Prescription | BOEHRINGER INGELHEIM | Valid |
| NIZORTAN PLUS | 40,12.5 mg,mg | Tablet · Oral use | 28 Blister | SAR 53.30 | Generic · Prescription | Tabuk Pharmaceutical Manufacturing Company | Valid |
| NIZORTAN PLUS | 80,12.5 mg,mg | Tablet · Oral use | 28 Blister | SAR 53.30 | Generic · Prescription | Tabuk Pharmaceutical Manufacturing Company | Valid |
| NIZORTAN PLUS | 80,25 mg,mg | Tablet · Oral use | 28 Blister | SAR 53.30 | Generic · Prescription | Tabuk Pharmaceutical Manufacturing Company | Valid |
| LISART PLUS 40 MG/12.5 MG TABLET | 40 , 12.5 mg | Tablet · Oral use | 28 Blister | SAR 59.20 | Generic · Prescription | RIYADH PHARMA | Withdrawn by MAH · Not Marketed |
| LISART PLUS 80 MG/12.5 MG TABLET | 80 , 12.5 mg | Tablet · Oral use | 28 Blister | SAR 59.20 | Generic · Prescription | RIYADH PHARMA | Withdrawn by MAH · Not Marketed |
Indications — CHI Daman Drug Formulary
HYPERTENSION
US FDA United States — FDA approvals (Drugs@FDA)
| Product | Strength | Form · route | Applicant | Status | First approved |
|---|---|---|---|---|---|
| CHLOROTHIAZIDE SODIUM | EQ 500MG BASE/VIAL | injectable · injection | FRESENIUS KABI USA | Prescription | 16 Oct 2009 |
| CHLOROTHIAZIDE SODIUM | EQ 500MG BASE/VIAL | injectable · injection | SUN PHARM | Prescription | 26 Jul 2011 |
| CHLOROTHIAZIDE SODIUM | EQ 500MG BASE/VIAL | injectable · injection | AM REGENT | Prescription | 22 Apr 2013 |
| CHLOROTHIAZIDE SODIUM | EQ 500MG BASE/VIAL | injectable · injection | SAGENT PHARMS INC | Prescription | 29 May 2015 |
| CHLOROTHIAZIDE SODIUM | EQ 500MG BASE/VIAL | injectable · injection | GLAND | Prescription | 3 Oct 2024 |
| DIURIL | 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**; 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | tablet · oral | RISING | Discontinued | 4 Sep 1958 |
| DIURIL | EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | injectable · injection | RISING | Discontinued | 4 Sep 1958 |
| DIURIL | 250MG/5ML | suspension · oral | SALIX PHARMS | Discontinued | 6 Oct 1961 |
| CHLOROTHIAZIDE | 500MG; 250MG | tablet · oral | PHARMOBEDIENT | Discontinued | 17 Jul 1975 |
| CHLOROTHIAZIDE | 250MG | tablet · oral | WATSON LABS | Discontinued | 4 Nov 1977 |
| CHLOROTHIAZIDE | 250MG | tablet · oral | ABC HOLDING | Discontinued | 8 Mar 1978 |
| CHLOROTHIAZIDE | 250MG | tablet · oral | SANDOZ | Discontinued | 1 Apr 1981 |
| CHLOROTHIAZIDE | 250MG | tablet · oral | HIKMA INTL PHARMS | Discontinued | 14 Jul 1982 |
| CHLOROTHIAZIDE | 500MG | tablet · oral | HIKMA INTL PHARMS | Discontinued | 14 Jul 1982 |
| CHLOROTHIAZIDE | 250MG | tablet · oral | WATSON LABS | Discontinued | 15 Aug 1983 |
| CHLOROTHIAZIDE SODIUM | EQ 500MG BASE/VIAL | injectable · injection | RK PHARMA | Discontinued | 18 Jun 2014 |
| CHLOROTHIAZIDE | 500MG | tablet · oral | WATSON LABS | Discontinued | |
| CHLOROTHIAZIDE | 250MG | tablet · oral | WATSON LABS | Discontinued | |
| CHLOROTHIAZIDE | 500MG | tablet · oral | WATSON LABS | Discontinued | |
| CHLOROTHIAZIDE | 500MG | tablet · oral | LEDERLE | Discontinued | |
| CHLOROTHIAZIDE | 250MG | tablet · oral | LEDERLE | Discontinued |
WHO WHO Model List of Essential Medicines (2025)
- 12.3. Antihypertensive medicines · core
Therapeutic equivalent to hydrochlorothiazide for Essential hypertension - 12.4. Medicines used in heart failure · core
Therapeutic equivalent to hydrochlorothiazide for Heart failure
Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.