| ID | 1775 |
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| No | 1775 |
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| Brand Name | LUCIPRET |
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| Ingredients | PRETOMANID 200 MG |
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| Dosage Form | TABLET |
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| Primary Packaging | BOTTLE |
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| Storage | |
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| Shelf Life | 2 YEARS |
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| Pack Size | BOX OF 30'S/BOTTLE |
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| Dispensing Category | |
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| ATC Classification | |
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| Pharmaceutical Class | |
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| Indications | AS PART OF A COMBINATION REGIMEN WITH BEDAQUILINE AND LINEZOLID FOR THE TREATMENT OFADULTS WITH PULMONARY EXTENSIVELY DRUG RESISTANT, TREATMENT INTOLERANT OR NONRESPONSIVE MULTIDRUG RESISTANT TUBERCULOSIS. |
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| Contraindications | |
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| Side Effects | |
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| Unit Price | |
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| EDL | NULL |
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| Description | WHITE OVAL TABLET |
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| Note | |
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| License Owner | LUCIUS PHARMACEUTICALS(LAO) CO.,LTD |
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| Manufacturer | LUCIUS PHARMACEUTICALS(LAO) CO.,LTD |
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| Country | LAOS |
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| Import Registration No | |
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| Import Registration Date | |
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| Activity | CERTIFICATE RELEASED |
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| Applied Date | |
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| FDD Registration No | 04 L 1342/25 |
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| FDD Registration Date | 27/05/2025 |
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| Expiry Date | 26/05/2030 |
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