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HSA Approval

COZAAR TABLET 50 mg

SIN08588P

COZAAR TABLET 50 mg

COZAAR TABLET 50 mg

March 8, 1996

ORGANON SINGAPORE PTE. LTD.

ORGANON SINGAPORE PTE. LTD.

Regulatory Information

HSA regulatory responsibility and product classification details

Regulatory Responsibility

RegistrantORGANON SINGAPORE PTE. LTD.
Licence HolderORGANON SINGAPORE PTE. LTD.

Product Classification

D
Drug Type
Therapeutic
F
Forensic Class
Prescription Only
HSA Singapore Classification

Formulation Information

TABLET, FILM COATED

**III. DOSAGE AND ADMINISTRATION** COZAAR may be administered with or without food. COZAAR may be administered with other antihypertensive agents. **Hypertension** The usual starting and maintenance dose is 50 mg once daily for most patients. The maximal antihypertensive effect is attained 3–6 weeks after initiation of therapy. Some patients may receive an additional benefit by increasing the dose to 100 mg once daily. For patients with intravascular volume-depletion (e.g., those treated with high-dose diuretics), a starting dose of 25 mg once daily should be considered (see PRECAUTIONS – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_). No initial dosage adjustment is necessary for elderly patients up to 75 years of age, or for patients with mild renal impairment. For patients above 75 years of age, patients with moderate to severe renal impairment and patients on dialysis, a lower starting dose of 25 mg is recommended. A lower dose should be considered for patients with a history of hepatic impairment (see PRECAUTIONS – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_). **Reduction in the Risk of Stroke in Hypertensive Patients with Left Ventricular Hypertrophy** The usual starting dose is 50 mg of COZAAR once daily. A low dose of hydrochlorothiazide should be added and/or the dose of COZAAR should be increased to 100 mg once daily based on blood pressure response. **Renal Protection in Type 2 Diabetic Patients with Proteinuria** The usual starting dose is 50 mg once daily. The dose may be increased to 100 mg once daily based on blood pressure response. COZAAR may be administered with other antihypertensive agents (e.g., diuretics, calcium channel blockers, alpha- or beta-blockers, and centrally acting agents) as well as with insulin and other commonly used hypoglycemic agents (e.g., sulfonylureas, glitazones and glucosidase inhibitors).

ORAL

Medical Information

**II. INDICATIONS** **Hypertension** COZAAR is indicated for the treatment of hypertension. **Hypertensive Patients with Left Ventricular Hypertrophy** COZAAR is indicated for the reduction in the risk of stroke in hypertensive patients with left ventricular hypertrophy (see RACE – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_). **Renal Protection in Type 2 Diabetic Patients with Proteinuria** COZAAR is indicated to delay the progression of renal disease as measured by a reduction in the incidence of doubling of serum creatinine and end stage renal disease (need for dialysis or renal transplantation), and to reduce proteinuria.

**IV. CONTRAINDICATIONS** COZAAR is contraindicated in patients who are hypersensitive to any component of this product. The concomitant use of COZAAR with aliskiren-containing products is contraindicated in patients with diabetes mellitus or renal impairment (GFR <60 mL/min/1.73 m2) (see DRUG INTERACTIONS – _please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information_).

C09CA01

losartan

Manufacturer Information

ORGANON SINGAPORE PTE. LTD.

Organon Pharma (UK) Limited

PT Organon Pharma Indonesia Tbk (Primary and Secondary Packager)

Active Ingredients

LOSARTAN POTASSIUM

50 mg

Losartan

Documents

Package Inserts

Cozaar_PI.pdf

Approved: December 28, 2022

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