View drug registration information details.
| Items | Registration information |
|---|
| ID | 788 |
|---|
| No | 788 |
|---|
| Brand Name | DEXTROSE SODIUM CHLORIDE 1/3 |
|---|
| Ingredients | DEXTROSE ANHYDROUS 5000MG,SODIUM CHLORIDE 300MG |
|---|
| Dosage Form | INFUSION |
|---|
| Primary Packaging | Sachet |
|---|
| Storage | |
|---|
| Shelf Life | 4 YEAR |
|---|
| Pack Size | 500ML,1000ML/SACHET/PLASTIC |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | - |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | CLEAR,STERILE SOLUTION ,PEROGEN FREE |
|---|
| Note | |
|---|
| License Owner | FACTORY NO. 3 |
|---|
| Manufacturer | FACTORY NO. 3 |
|---|
| Country | LAO PDR |
|---|
| Import Registration No | |
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| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 11 L 0543/08 |
|---|
| FDD Registration Date | 15-Dec-2023 |
|---|
| Expiry Date | 14-Dec-2026 |
|---|
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