View drug registration information details.
| Items | Registration information |
|---|
| ID | 1622 |
|---|
| No | 1622 |
|---|
| Brand Name | ALLIBUFEN |
|---|
| Ingredients | IBUPROFEN 400 MG |
|---|
| Dosage Form | TABLET |
|---|
| Primary Packaging | BLISTERPACK |
|---|
| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | BOX OF 2 X 10'S, 50 X 10'S |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | MILD TO MODERATE PAIN, FEVER, RHEUMATIC DISEASE |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | YELLOW TABLET |
|---|
| Note | |
|---|
| License Owner | LAOS ALLIANCE PHARMACEUTICAL GROUP COMPANY |
|---|
| Manufacturer | LAOS ALLIANCE PHARMACEUTICAL GROUP COMPANY |
|---|
| Country | LAOS |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 10 L 0925/22 |
|---|
| FDD Registration Date | 26-FEB-2025 |
|---|
| Expiry Date | 25-FEB-2030 |
|---|
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