View drug registration information details.
Items | Registration information |
ID | 949 |
No | 949 |
Brand Name | PHOLENVA 4 |
Ingredients | LENVATINIB 4 MG |
Dosage Form | CAPSULE |
Primary Packaging | BLISTERPACK |
Storage | STORE IN DRY PLACE , AT TEMPERATURE 15-30 C, PROTECT FROM LIGHT |
Shelf Life | 3 YEARS |
Pack Size | BOX OF 3 X 10'S |
Dispensing Category | Prescription only |
ATC Classification | |
Pharmaceutical Class | ANTINEOPLASTIC |
Indications | FOR THE TREATMENT OF PATIENTS WITH LOCALLY RECURRENT OR METASTATIC, PROGRESSIVE, RADIOACTIVE IODINE REFRACTORY DIFFERENTIATED THYROID CANCER |
Contraindications | NONE |
Side Effects | HYPERTENSION, CARDIAC DYSFUNCTION, HEPATOTOXICITY, PROTEINUREA, DIARREA, HYPOCALCEMIA, HEMORRHAGIC EVENT |
Unit Price | |
EDL |
No |
Description | WHITE-YELLOW CAPSULE CONTAINING WHITE GRANULES |
Note | |
License Owner | FACTORY NO.2 |
Manufacturer | FACTORY NO. 2 |
Country | LAO PDR |
Import Registration No | 02 L 0823/20 |
Import Registration Date | 2020-02-01 |
Activity | CERTIFICATE RELEASED |
Applied Date | |
FDD Registration No | 02 L 0823/20 |
FDD Registration Date | 2023-08-29 |
Expiry Date | 2026-08-28 |
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