View drug registration information details.
| Items | Registration information |
|---|
| ID | 1690 |
|---|
| No | 1690 |
|---|
| Brand Name | LUCIBARIC |
|---|
| Ingredients | BARICITINIB 2 MG |
|---|
| Dosage Form | TABLET |
|---|
| Primary Packaging | BOTTLE |
|---|
| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | BOX OF 30'S/BOTTLE |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | FOR THE TREATMENT OF ADULT PATIENTS WITH MODERATELY TO SEVERELY ACTIVE RHEUMATOID ARHTRITIS WHO HAVE HAD AN INADEQUATE RESPONSE TO ONE OR MORE TNF BLOCKERS, FOR THE TREATMENT OF ADULT PATIENTS WITH SEVERE ALOPECIA AREATA. |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | PINK FILM COATED TABLET, WITH LETTER LUS ON ONE SIDE |
|---|
| Note | |
|---|
| License Owner | LUCIUS PHARMACEUTICALS(LAO) CO.,LTD |
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| Manufacturer | LUCIUS PHARMACEUTICALS(LAO) CO.,LTD |
|---|
| Country | LAOS |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 03 L 1311/25 |
|---|
| FDD Registration Date | 07-APR-2025 |
|---|
| Expiry Date | 06-APR-2030 |
|---|
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