View drug registration information details.
| Items | Registration information |
|---|
| ID | 1010 |
|---|
| No | 1010 |
|---|
| Brand Name | SODIUM CHLORIDE 20% |
|---|
| Ingredients | SODIUM CHLORIDE 2000MG |
|---|
| Dosage Form | INJECTION |
|---|
| Primary Packaging | AMPOULES |
|---|
| Storage | |
|---|
| Shelf Life | 4 YEARS |
|---|
| Pack Size | 10ML/AMP, 50 AMPS/BOX |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | IS INDICATED IN STATES OF SODIUM DEPLETION AND USUALLY NEEDS TO BE GIVEN INTRAVENOUSLY |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | CLEAR STERILE SOLUTION |
|---|
| 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 | 07 L 0187/96 |
|---|
| FDD Registration Date | 23-JUN-2025 |
|---|
| Expiry Date | 22-JUN-2030 |
|---|
Back to drug list
|
