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