View drug registration information details.
| Items | Registration information |
|---|
| ID | 2299 |
|---|
| No | 2299 |
|---|
| Brand Name | DICLOFENAC 50 MG |
|---|
| Ingredients | DICLOFENAC SODIUM 50 MG |
|---|
| Dosage Form | TABLET |
|---|
| Primary Packaging | ALU-BLISTER |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | BOX OF 50 X 10'S |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | RHEUMATOID ARTHRITIS, OSTEO-ARTHRITIS AND ANKYLOSING SPONDYLITIS, POST TRAUMATIC PAIN AND INFLAMMATION, SYMPTOMATIC TREATMENT OF PRIMARY DYSMENORRHOEA. |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | WHITE FILM COATED TABLET |
|---|
| Note | |
|---|
| License Owner | SOKDY OSOTH IMPORT-EXPORT CO., LTD |
|---|
| Manufacturer | JIANGSU RUINIAN QIANJIN PHARMACEUTICAL CO.,LTD |
|---|
| Country | CHINA |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 05 I 5499/23 |
|---|
| FDD Registration Date | 09-MAY-2023 |
|---|
| Expiry Date | 08-MAY-2026 |
|---|
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