| ID | 21 |
|---|
| No | 21 |
|---|
| Brand Name | AMLOD 10 |
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| Ingredients | AMLODIPINE BESYLATE 13.868 MG EQ TO AMLODIPINE 10 MG |
|---|
| Dosage Form | TABLET |
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| Primary Packaging | ALU-PVC/PVDC BLISTERPACK |
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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 10 X 10'S |
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| Dispensing Category | PRESCRIPTION ONLY |
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| ATC Classification | C02DE12 |
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| Pharmaceutical Class | ANTIHYPERTENSIVES |
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| Indications | FOR THE TREATMENT OF CHRONIC STABLE ANGINA, OF CONFIRMED OR SUSPECTED VASOSPASTIC ANGINA AND HYPERTENSION. |
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| Contraindications | EXCEPT UNDER SPECIAL CIRCUMSTANCES, THIS MEDICATION SHOULD NOT BE USED WHEN THE FOLLOWING MEDICAL PROBLEM EXST: SEVERE HYPERTENSION, AORTIC STENOSIS |
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| Side Effects | PERIPHERAL EDEMA, DIZZINESS LESS FREQUENT. |
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| Unit Price | - |
|---|
| EDL |
Yes |
|---|
| Description | WHITE, OCTAGONAL, FLAT TABLET , BEVELLED ON BOTH SIDE WITH ENGRAVED A- 10 ON ONE SIDE AND SCORED ON THE OTHER |
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| Note | |
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| License Owner | AI KEN PHARMA CO., LTD |
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| Manufacturer | UNISON LABORATORIES CO., LTD |
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| Country | THAILAND |
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| Import Registration No | 1A 45/50 (NG) |
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| Import Registration Date | 25/07/2007 |
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| Activity | CERTIFICATE RELEASED |
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| Applied Date | 2022-09-28 |
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| FDD Registration No | 05 I 4152/16 |
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| FDD Registration Date | 2023-02-02 |
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| Expiry Date | 2026-02-01 |
|---|
