| ID | 1601 |
|---|
| No | 1601 |
|---|
| Brand Name | ALIGIRITINIB |
|---|
| Ingredients | GILTERITINIB FUMARATE 40 MG |
|---|
| Dosage Form | TABLET |
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| Primary Packaging | BOTTLE |
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| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | 90 CAPSULES/BOTTLE |
|---|
| Dispensing Category | |
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| ATC Classification | |
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| Pharmaceutical Class | |
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| Indications | FOR THE TREATMENT OF ADULT PATIENTS WHO HAVE RELAPSED OR REFRACTORY ACUTE MYELOID LEUKEMIA WITH AN FMS-LIKE TYROSINE KINASE 3 MUTATION |
|---|
| Contraindications | |
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| Side Effects | |
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| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | YELLOW PLAT TABLETS |
|---|
| Note | |
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| License Owner | LAOS ALLIANCE PHARMACEUTICAL GROUP COMPANY |
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| Manufacturer | LAOS ALLIANCE PHARMACEUTICAL GROUP COMPANY |
|---|
| Country | LAOS |
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| Import Registration No | |
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| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 11 L 1234/24 |
|---|
| FDD Registration Date | 14-NOV-2024 |
|---|
| Expiry Date | 13-NOV-2029 |
|---|
