| ID | 1708 |
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| No | 1708 |
|---|
| Brand Name | LUCIDAC |
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| Ingredients | DACOMITINIB 15 MG |
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| Dosage Form | FILM COATED 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 | TREATMENT OF PATIENTS WITH METASTATIC NON SMALL CELL LUNG CANCER WITH EPIDERMAL GROWTH FACTOR RECEPTOR EXON 19 DELETION OR EXON 21 L858R SUBSTITUTION MUTATION |
|---|
| Contraindications | |
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| Side Effects | |
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| Unit Price | |
|---|
| EDL | NULL |
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| Description | LIGHT BLUE, FILM COATED 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 |
|---|
| Applied Date | |
|---|
| FDD Registration No | 06 L 1115/24 |
|---|
| FDD Registration Date | 21/06/2024 |
|---|
| Expiry Date | 20/06/2027 |
|---|
