| ID | 381 |
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| No | 381 |
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| Brand Name | AMOXICILLIN AND CLAVULANATE POTASSIUM TABLET 625 MG |
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| Ingredients | AMOXICILLIN SODIUM EQ.TO AMOXICILLIN 500 MG, CLAVULANATE POTASSIUM EQ.TO CLAVULANIC ACID 125 MG |
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| Dosage Form | TABLET |
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| Primary Packaging | BLISTERPACK |
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| Storage | STORE IN A DRY PLACE, BELOW 30 C, PROTECT FROM LIGHT |
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| Shelf Life | 3 YEARS |
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| Pack Size | BOX OF 2 BLISTERS X 7 TABLETS |
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| Dispensing Category | Prescription only |
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| ATC Classification | |
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| Pharmaceutical Class | ANTIBACTERIAL COMBINATIONS |
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| Indications | UPPER AND LOWER RESPIRATORY TRACT INFECTION, GENITOURINARY TRACT INFECTION, SKIN AND SOFT TISSUE INFECTION, BONE AND JOINT INFECTION, |
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| Contraindications | PATIENTS WITH PENICILLIN POSITIVE SKIN TEST OR PATIENT WITH HISTORY OF ALLERGIC TO PENICILLIN OR INFECTIOUS MONOCYTOSIS |
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| Side Effects | DIARRHEA, NAUSEA, VOMITING |
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| Unit Price | 0.4 |
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| EDL |
Yes |
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| Description | OVAL, FILM COATED TABLET, A BREAKLINE ON ONE SIDE |
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| Note | |
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| License Owner | NAKORNLUANG PHARMA EXPORT-IMPORT CO.,LTD |
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| Manufacturer | REYOUNG PHARMACEUTICAL CO.,LTD |
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| Country | CHINA |
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| Import Registration No | H19994051 |
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| Import Registration Date | 2020-03-25 |
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| Activity | CERTIFICATE RELEASED |
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| Applied Date | 2024-04-26 |
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| FDD Registration No | 01 I 5870/25 |
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| FDD Registration Date | 2025-01-31 |
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| Expiry Date | 2030-01-30 |
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