View drug registration information details.
| Items | Registration information |
|---|
| ID | 1501 |
|---|
| No | 1501 |
|---|
| Brand Name | IBUMAN-400 |
|---|
| Ingredients | IBUPROFEN 400 MG |
|---|
| Dosage Form | FILM-COATED TABLETS |
|---|
| Primary Packaging | PVC-ALU BLISTERPVC-ALU BLISTER & BOTTLE |
|---|
| Storage | |
|---|
| Shelf Life | 4 YEARS |
|---|
| Pack Size | BOX OF 100 X 10'S, 500’S/BOTTLE |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | FOR RELIEF SYMPTOMS IN RHEUMATIC DISORDERS SUCH AS OSTEOARTHRITIS AND RHEUMATOID ARTHRITIS |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | AN OBLONG SHAPE, VIOLET COLOR, FILM COATED TABLET, ENGRAVING A MANUFACTURER TRADEMARK ON ONE SIDE |
|---|
| Note | |
|---|
| License Owner | LAO INTER PHARMA CO.,LTD |
|---|
| Manufacturer | T.MAN PHARMA CO.,LTD |
|---|
| Country | THAILAND |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 09 I 5141/21 |
|---|
| FDD Registration Date | 10-FEB-2025 |
|---|
| Expiry Date | 09-FEB-2030 |
|---|
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