View drug registration information details.
Items | Registration information |
ID | 217 |
No | 217 |
Brand Name | BARUDX |
Ingredients | BARICITINIB 4 MG |
Dosage Form | FILM COATED TABLET |
Primary Packaging | BOTTLE |
Storage | STORE BELOW 30 C |
Shelf Life | 2 YEARS |
Pack Size | BOX OF 28'S/BOTTLE |
Dispensing Category | PRESCRIPTION |
ATC Classification | |
Pharmaceutical Class | ANTINEOPLASTIC |
Indications | TO TREAT RHEUMATOID ARTHRITIS (CONDITION IN WHICH THE BODY ATTACKS ITS OWN JOINTS CAUSING PAIN, SWELLING, AND LOSS OF FUNCTION) IN ADULT WHO HAVE NOT RESPONDED WELL TO ONBE OR MORE TUMOR NECROSIS FACTOR INHOBITOR MEDICATION. |
Contraindications | |
Side Effects | |
Unit Price | |
EDL |
No |
Description | LIGHT PINK, ROUND, EMBOSSED DX ON ONE SIDE AND 4 ON THE OTHER SIDE |
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 | 03 L 1084/24 |
FDD Registration Date | 2024-03-29 |
Expiry Date | 2027-03-28 |
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