| ID | 403 |
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| No | 403 |
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| Brand Name | ACETAN HCT TABLET 50/12.5 MG |
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| Ingredients | LOSARTAN POTASSIUM EQ.TO LOSARTAN 50 MG, HYDROCHLOROTHIAZIDE 12.5 MG |
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| Dosage Form | FILM COATED TABLET |
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| Primary Packaging | PVC BLISTER |
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| Storage | STORE AT TEMPERATURE NOT MORE THAN 30 C |
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| Shelf Life | 3 YEARS |
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| Pack Size | BOX OF 3 X 10'S |
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| Dispensing Category | PRESCRIPTION ONLY |
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| ATC Classification | C09DA01 |
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| Pharmaceutical Class | ANTIHYPERTENSIVES |
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| Indications | FOR THE TREATMENT OF HYPERTENSION, FOR PATIENTS IN WHOM COMBINATION THERAPY IS APPROPRIATE, TO REDUCE THE RISK OF STROKE IN PATIENTS WITH HYPERTENSION AND LEFT VENTRICULAR HYPERTHROPHY BUT THERE IS EVIDENCE THAT THIS BENEFIT DOES NOT APPLY TO BLACK PATIENTS. |
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| Contraindications | PATIENTS WHO ARE HYPERSENSITIVITY TO ANY COMPONETN OF THIS PRODUCT, PATIENT WITH ANURIA AND HYPERSENSITIVITY TO OTHER SULFONAMIDE-DERIVED DRUGS |
|---|
| Side Effects | DIZZINESS, ASTHENIA, FATIGUE, VERTIGO., |
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| Unit Price | |
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| EDL |
No |
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| Description | AN ELLIPSE, LIGHT YELLOW COLOR FILM COATED TABLET WITH ACE ON ONE SIDE AND 50 ON OTHER SIDE |
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| Note | |
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| License Owner | DKSH LAOS COMPANY LIMITED |
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| Manufacturer | DUOPHARMA MANUFACTURING(BANGI)SDN.BHD. |
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| Country | MALAYSIA |
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| Import Registration No | MAL12085071AZ |
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| Import Registration Date | 2012-08-30 |
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| Activity | CERTIFICATE RELEASED |
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| Applied Date | 2022-04-22 |
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| FDD Registration No | 07 I 5579/23 |
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| FDD Registration Date | 2023-07-07 |
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| Expiry Date | 2026-07-06 |
|---|
