View the MAGNESIUM SULFATE registration information details.
| Items | Drug Registration information |
|---|
| ID | 807 |
|---|
| No | 807 |
|---|
| Brand Name | MAGNESIUM SULFATE |
|---|
| Ingredients | MAGNESIUM SULFATE 5 G |
|---|
| Dosage Form | INJECTION |
|---|
| Primary Packaging | AMPOULES |
|---|
| Storage | |
|---|
| Shelf Life | - |
|---|
| Pack Size | BOX OF 50 X 10ML |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | HYPOMAGNESEMIA TREATMENT |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL | NULL |
|---|
| Description | STERILE SOLUTION |
|---|
| Note | |
|---|
| License Owner | FACTORY NO. 3 |
|---|
| Manufacturer | FACTORY NO. 3 |
|---|
| Country | LAO PDR |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 11 L 0835/20 |
|---|
| FDD Registration Date | 29/07/2024 |
|---|
| Expiry Date | 28/07/2027 |
|---|
