| Items | Drug Registration information |
|---|---|
| ID | 875 |
| No | 875 |
| Brand Name | BARICMAKS |
| Ingredients | BARICITINIB 4 MG |
| Dosage Form | TABLET |
| Primary Packaging | BOTTLE |
| Storage | |
| Shelf Life | 3 YEARS |
| Pack Size | 30 TABLETS/BOTTLE |
| Dispensing Category | |
| ATC Classification | |
| Pharmaceutical Class | |
| Indications | FOR THE TREATMENT OF ADULT PATIENTS WITH MODERATELY TO SEVERELY ACTIVE RHEUMATOID ARHTRIS WHO HAVE HAD AN INADEQUATE RESPONSE TO ONE OR MORE TUMOR NECROSIS FACTOR BLOCKER |
| Contraindications | |
| Side Effects | |
| Unit Price | |
| EDL | NULL |
| Description | LIGHT YELLOW , FILM COATED TABLET |
| 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 | 04 L1349/25 |
| FDD Registration Date | 30/04/2025 |
| Expiry Date | 29/04/2030 |