View drug registration information details.
| Items | Registration information |
|---|
| ID | 999 |
|---|
| No | 999 |
|---|
| Brand Name | REPOTREMAKS |
|---|
| Ingredients | REPOTRECTINIB 40 MG |
|---|
| Dosage Form | CAPSULE |
|---|
| Primary Packaging | BOTTLE |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | BOX OF 60'S |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | LOCALLY ADVANCED OR METASTATIC ROS1-POSITIVE NON SMALL CELL LUNG CANCER |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | WHITE CAPSULE CONTAINS WHITE POWDER |
|---|
| Note | |
|---|
| License Owner | FACTORY NO.2 |
|---|
| Manufacturer | FACTORY NO. 2 |
|---|
| Country | LAOS |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 07 L 1145/24 |
|---|
| FDD Registration Date | 12-JUL-2024 |
|---|
| Expiry Date | 11-JUL-2027 |
|---|
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