View drug registration information details.
| Items | Registration information |
|---|
| ID | 231 |
|---|
| No | 231 |
|---|
| Brand Name | ERDADX |
|---|
| Ingredients | ERDAFITINIB 4 MG |
|---|
| Dosage Form | FILM COATED TABLET |
|---|
| Primary Packaging | BOTTLE |
|---|
| Storage | STORE AT 20-25 C |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | BOX OF 56'S/BOTTLE |
|---|
| Dispensing Category | PRESCRIPTION |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | ANTINEOPLASTIC |
|---|
| Indications | TO TREAT CERTAIN TYPES OF UROTHELIAL CANCER |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
No |
|---|
| Description | ORANGE TABLETS |
|---|
| Note | |
|---|
| License Owner | BIGBEAR PHARMACEUTICAL LAO CO.,LTD |
|---|
| Manufacturer | BIGBEAR PHARMACEUTICAL LAO CO.,LTD |
|---|
| Country | LAOS |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 07 L 0992/23 |
|---|
| FDD Registration Date | 2023-07-31 |
|---|
| Expiry Date | 2026-07-30 |
|---|
Back to drug list
|
