View drug registration information details.
| Items | Registration information |
|---|
| ID | 50 |
|---|
| No | 50 |
|---|
| Brand Name | MEMXA 10 |
|---|
| Ingredients | MEMANTINE HYDROCHLORIDE 10 MG EQ.TO MEMANTINE 8.310 MG |
|---|
| Dosage Form | FILM-COATED TABLETS |
|---|
| Primary Packaging | ALU-PVC/PVDC |
|---|
| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | BOX OF 3 X 10'S |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | TREATMENT OF PATIENTS WITH MODERATE TO SEVERE ALZHEIMER'S DISEASE |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | WHITE, CENTRALLY, TAPERED OBLONG, BICONVEX, FILM COATED TABLET WITH ENGRAVED MMT ON ONE SIDE AND SCORED 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 | 06 I 4709/19 |
|---|
| FDD Registration Date | 5-AUG-2022 |
|---|
| Expiry Date | 4-AUG-2025 |
|---|
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