View drug registration information details.
| Items | Registration information |
|---|
| ID | 810 |
|---|
| No | 810 |
|---|
| Brand Name | MANNITOL |
|---|
| Ingredients | D-MANNITOL 20 % |
|---|
| Dosage Form | INFUSION |
|---|
| Primary Packaging | BAG |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | 500 ML/BAG (20 BAGS/CARTON), 1000 ML/BAG (10 BAGS/CARTON) |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | to decrease pressure in the eyes, as in glaucoma, and to lower increased intracranial pressure |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | CLEAR COLORLESS 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 | 01 L 1289/25 |
|---|
| FDD Registration Date | 03-FEB-2025 |
|---|
| Expiry Date | 02-FEB-2030 |
|---|
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