View drug registration information details.
| Items | Registration information |
|---|
| ID | 2586 |
|---|
| No | 2586 |
|---|
| Brand Name | DICLOFENAC SODIUM |
|---|
| Ingredients | DICLOFENAC SODIUM 50 MG |
|---|
| Dosage Form | TABLET |
|---|
| Primary Packaging | BLISTERPACK |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | 10 TABS/BLIST., 50 BLISTS/BOX |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | INDICATED FOR ACUTE AND CHRONIC TREATMENT OF SIGNS AND SYMPTOMS OF RHEUMATOID ARTHRITIS, OSTEOARTHRITIS AND ANKYLOSING SPONDYLITIS. USED ALSO IN MUSCULAR PAIN, BURSITIS, TRAUMATIC PAIN, TOOTHACHE, MENORRHAGIA AND HEADACHE |
|---|
| Contraindications | |
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| Side Effects | |
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| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | AN ENTERIC-COATED TABLETS WITH WHITE CORE |
|---|
| Note | |
|---|
| License Owner | VIENGCHALEUN PHARMA IMPORT-EXPORT COMPANY |
|---|
| Manufacturer | SHANXI SHUGUANG PHARMACEUTICAL CO.,LTD |
|---|
| Country | CHINA |
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| Import Registration No | |
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| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 06 I 3076/08 |
|---|
| FDD Registration Date | 08-APR-2024 |
|---|
| Expiry Date | 07-APR-2027 |
|---|
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