View drug registration information details.
| Items | Registration information |
|---|
| ID | 36 |
|---|
| No | 36 |
|---|
| Brand Name | LECETAM 500 |
|---|
| Ingredients | LEVETIRACETAM 500 MG |
|---|
| Dosage Form | FILM-COATED TABLETS |
|---|
| Primary Packaging | ALU-ALU BLISTERPACK |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | BOX OF 6 X 10'S |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | AS MONOTHERAPY IN THE TREATMENT OF PARTIAL ONSET SEIZURES WITH OR WITHOUT SECONDARY GENERALIZATION IN ADULTS AND ADOLESCENTS FROM 16 YEARS OF AGE WITH NEWLY DIAGNOSED EPILEPSY. |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | YELLOW. OBLONG, BICONVEX, FILM COATED TABLET WITH ENGRAVED "L-500"ON ONE SIDE AND PLAIN ON THE OTHER |
|---|
| Note | |
|---|
| License Owner | AI KEN PHARMA CO., LTD |
|---|
| Manufacturer | UNISON LABORATORIES CO., LTD |
|---|
| Country | THAILAND |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 12 I 4879/19 |
|---|
| FDD Registration Date | 2-Feb-2023 |
|---|
| Expiry Date | 01-Feb-2026 |
|---|
Back to drug list
|
