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LOSARTAN HEXAL 100MG FILM-COATED TABLETS [SIN13851P]
Active ingredients: LOSARTAN HEXAL 100MG FILM-COATED TABLETS
Last updated 26 October 2025
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Product Info
LOSARTAN HEXAL 100MG FILM-COATED TABLETS
[SIN13851P]
Product information
Active Ingredient and Strength | LOSARTAN POTASSIUM EQV LOSARTAN 91.52 MG - 100 MG |
Dosage Form | TABLET, FILM COATED |
Manufacturer and Country | GENVEON ILAC SANAYI VE TICARET A.S. (GEBZE 1) - TURKEY |
Registration Number | SIN13851P |
Licence Holder | SANDOZ SINGAPORE PTE. LTD. |
Forensic Classification | PRESCRIPTION ONLY MEDICINES |
Anatomical Therapeutic Chemical (ATC) code | C09CA01 |
4.1 Therapeutic indications
Losartan is indicated for the treatment of hypertension.
Losartan is indicated for the reduction in the risk of stroke in hypertensive patients with left ventricular hypertrophy (see section 5.1 – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).
Losartan 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 (see section 5.1 – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).
4.2 Posology and method of administration
Posology
Losartan 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 section 4.4 – 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 section 4.4 – 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
The usual starting dose is 50 mg once daily.
The dose may be increased to 100 mg once daily based on blood pressure response.
Losartan 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 hypoglycaemic agents (e.g., sulfonylureas, glitazones and glucosidase inhibitors).
Reduction in the Risk of Stroke in Hypertensive Patients with Left Ventricular Hypertrophy
The usual starting dose is 50 mg of Losartan once daily. A low dose of hydrochlorothiazide should be added and/or the dose of Losartan should be increased to 100 mg once daily based on blood pressure response.
Method of administration
Losartan should be swallowed with a glass of water.
Losartan may be administered with or without food.
4.3 Contraindications
Losartan is contraindicated in patients who are hypersensitive to any component of this product.
The concomitant use of losartan with aliskiren-containing products is contraindicated in patients with diabetes mellitus or renal impairment (GFR <60 mL/min/1.73 m2) (see section 4.5 – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).