| ID | 1736 |
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| No | 1736 |
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| Brand Name | LUCIGEFI 250 MG |
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| Ingredients | GEFITINIB 250 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 | FOR THE FIRST LINE TREATMENT OF PATIENTS WITH METASTATIC NON SMALL CELL LUNG CANCER WHOSE TUMORS HAVE EPIDERMAL GROWTH FACTOR RECEPTOR EXON 19 DELETIONS OR EXON 21 |
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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 | BROWNISH ROUNF 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 | |
|---|
| FDD Registration No | 09 L 1215/24 |
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| FDD Registration Date | 31/10/2024 |
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| Expiry Date | 30/10/2029 |
|---|
