View drug registration information details.
| Items | Registration information |
|---|
| ID | 1014 |
|---|
| No | 1014 |
|---|
| Brand Name | DICLOFENAC |
|---|
| Ingredients | DICLOFENAC SODIUM 50MG |
|---|
| Dosage Form | TABLET |
|---|
| Primary Packaging | Bottle |
|---|
| Storage | - |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | 500,1000TABS/BOTTLE |
|---|
| Dispensing Category | Over the counter |
|---|
| ATC Classification | M01 |
|---|
| Pharmaceutical Class | ANTI-INFLAMMATORY ENZYMES |
|---|
| Indications | DICLOFENAC SODIUM HAS ANALGESIC, ANTIPYRETIC AND ANTI-INFLAMMATORY |
|---|
| Contraindications | - |
|---|
| Side Effects | - |
|---|
| Unit Price | - |
|---|
| EDL |
Yes |
|---|
| Description | PINK FILM COATED TABLET ON ONE SIDE HAVE A LINE AND OTHER SIDE HAVE WORD " PDC" |
|---|
| Note | |
|---|
| License Owner | FACTORY NO. 3 |
|---|
| Manufacturer | FACTORY NO. 3 |
|---|
| Country | LAO PDR |
|---|
| Import Registration No | 05 L 0272/98 |
|---|
| Import Registration Date | 1998-05-04 |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | 2023-03-17 |
|---|
| FDD Registration No | 05 L 0272/98 |
|---|
| FDD Registration Date | 2023-08-21 |
|---|
| Expiry Date | 2026-08-20 |
|---|
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