| ID | 440 |
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| No | 440 |
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| Brand Name | BEZARTAN TABLET 300 MG |
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| Ingredients | IRBESARTAN 300 MG |
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| Dosage Form | FILM COATED TABLET |
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| Primary Packaging | PVDC-BLISTER |
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| Storage | STORE AT THE TEMPERATURE BELOW 30 C AND PROTECT FROM LIGHT |
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| Shelf Life | 2 YEARS |
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| Pack Size | BOX OF 3 X 10'S |
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| Dispensing Category | PRESCRIPTION |
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| ATC Classification | C09CA04 |
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| Pharmaceutical Class | ANTIHYPERTENSIVE |
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| Indications | TREATMENT OF ESSENTIAL HYPERTENSION, TREATMENT OF DIABETIC NEPHROPATHY WITH AN ELEVATED SERUM CREATININE AND PROTEINURIA (>300 MG/DAY) IN PATIENTS WITH TYPE 2 DIABETES AND HYPERTENSION |
|---|
| Contraindications | HYPERSENSITIVITY, SECOND AND THIRD TRIMESTER OF PREGNANCY, WITH ALISKIREN-CONTAINING PRODUCT IN PATIENTS WITH DIABETE MELLITUS OR RENAL IMPAIREMENT |
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| Side Effects | HYPERKALAEMIA, DIZZINESS, ORTHOSTATIC DIZZINESS, NAUSEA, MUSCULOSKELETAL PAIN, FATIQUE |
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| Unit Price | |
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| EDL |
No |
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| Description | WHITE, OVAL-SHAPED, WITH SCORED ON ONE SIDE AND FILM COATED TABLET. |
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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 | MAL19056120AZ |
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| Import Registration Date | 2019-05-30 |
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| Activity | CERTIFICATE RELEASED |
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| Applied Date | 2021-12-03 |
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| FDD Registration No | 04 I 5476/23 |
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| FDD Registration Date | 2023-04-25 |
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| Expiry Date | 2026-04-24 |
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