View drug registration information details.
| Items | Registration information |
|---|
| ID | 2251 |
|---|
| No | 2251 |
|---|
| Brand Name | RHEUMETONE |
|---|
| Ingredients | NABUMETONE 500 MG |
|---|
| Dosage Form | FILM-COATED TABLETS |
|---|
| Primary Packaging | BLISTERPACK |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | BOX OF 10 X 10 TABLETS |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | OSTEOARTHRITIS AND RHEUMATOID ARTHRITIS REQUIRING ANTI-INFLAMMATORY ANALGESIC TREATMENT |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | PURPLE OBLONG SHAPE FILM COATED TABLET |
|---|
| Note | |
|---|
| License Owner | SENGSOUK PHARMACEUTICAL SOLE CO.,LTD |
|---|
| Manufacturer | THAI P.D.CHEMICALS CO.,LTD |
|---|
| Country | THAILAND |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 10 I 4812/19 |
|---|
| FDD Registration Date | 07-JUN-2023 |
|---|
| Expiry Date | 06-JUN-2026 |
|---|
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