View drug registration information details.
| Items | Registration information |
|---|
| ID | 859 |
|---|
| No | 859 |
|---|
| Brand Name | ALBENDAZOL |
|---|
| Ingredients | ALBENDAZOL 200MG |
|---|
| Dosage Form | TABLET |
|---|
| Primary Packaging | blisterpac |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | 2 TABLETS/BLIS/BOX, 10 BOX/PACK |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | FOR THE TREATMENT OF ALL WORM TYPE |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | WHITE BREAK LINE IN THE ONE SIDE AND NUMBER 2 MARK IN THE OTHER SIDE |
|---|
| 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 | 12 L 0350/01 |
|---|
| FDD Registration Date | 28-JUL-2022 |
|---|
| Expiry Date | 27-JUL-2025 |
|---|
Back to drug list
|
