View drug registration information details.
| Items | Registration information |
|---|
| ID | 629 |
|---|
| No | 629 |
|---|
| Brand Name | VIARTRIL-S |
|---|
| Ingredients | GLUCOSAMINE SULFATE 1500 MG, SODIUM CHLORIDE 384 MG |
|---|
| Dosage Form | POWDER FOR ORAL SOLUTION |
|---|
| Primary Packaging | SACHET |
|---|
| Storage | DO NOT STORE ABOVE 25 C |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | BOX OF30 SACHETS |
|---|
| Dispensing Category | Prescription only |
|---|
| ATC Classification | M01AX05 |
|---|
| Pharmaceutical Class | ANTIRHEUMATISM |
|---|
| Indications | TREATMENT OF OSTEOARTHRITIS AND /OR ITS SYMPTOMS I.E. PAIN AND FUNCTION LIMITATION |
|---|
| Contraindications | HYPERSENSITIVITY, PATIENTS WHO ARE ALLERGIC TO SHELLFISH |
|---|
| Side Effects | HEADACHE, SOMLOLENCE, DIARRHEA, CONSTIPATION, NAUSEA, FLATULENCE, ABDOMINAL PAIN, DYSPEPSIA, TIRENESS |
|---|
| Unit Price | |
|---|
| EDL |
No |
|---|
| Description | WHITE CRYSTALLINE ODORLESS POWDER |
|---|
| Note | |
|---|
| License Owner | DKSH LAOS COMPANY LIMITED |
|---|
| Manufacturer | ROTTAPHARM LTD |
|---|
| Country | IRELAND |
|---|
| Import Registration No | PA2010/022/002 |
|---|
| Import Registration Date | 1998-04-03 |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | 2021-07-01 |
|---|
| FDD Registration No | 04 I 5483/23 |
|---|
| FDD Registration Date | 2023-04-25 |
|---|
| Expiry Date | 2026-04-24 |
|---|
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