View drug registration information details.
| Items | Registration information |
|---|
| ID | 958 |
|---|
| No | 958 |
|---|
| Brand Name | ORAL |
|---|
| Ingredients | DEXTROSE ANHYDROUS 20G + SODIUM CHLORIDE 3.5G + SODIUM CITRATE 2.9G + POTASSIUM CHLORIDE 1.5G |
|---|
| Dosage Form | POWDER |
|---|
| Primary Packaging | Sachet |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | 27.9 G/ SACHET |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | FLUID AND ELECTROLYTE LOSS IN DIARRHOEA |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | WHITE POWDER IN ALUMINIUM SACHET |
|---|
| Note | |
|---|
| License Owner | FACTORY NO.2 |
|---|
| Manufacturer | FACTORY NO. 2 |
|---|
| Country | LAO PDR |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 08 L 0132/95 |
|---|
| FDD Registration Date | 11-DEC-2024 |
|---|
| Expiry Date | 10-DEC-2029 |
|---|
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