View drug registration information details.
| Items | Registration information |
|---|
| ID | 357 |
|---|
| No | 357 |
|---|
| Brand Name | SIALIS |
|---|
| Ingredients | TADALAFIL 10 MG |
|---|
| Dosage Form | TABLET |
|---|
| Primary Packaging | BLISTERPACK |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | BOX OF 2 X 2'S |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | USE FOR ERECTILE DYSFUNCTION AND BENIGN PROSTATIC HYPERPLASIA |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | YELLOW FILM COATED TABLET |
|---|
| Note | |
|---|
| License Owner | BOTEN ELEMENTO PHARMA FACTORY |
|---|
| Manufacturer | BOTEN ELEMENTO PHARMA FACTORY |
|---|
| Country | LAO PDR |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 03 L 0857/21 |
|---|
| FDD Registration Date | 06-Dec-2024 |
|---|
| Expiry Date | 05-Dec-2029 |
|---|
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