View drug registration information details.
| Items | Registration information |
|---|
| ID | 2653 |
|---|
| No | 2653 |
|---|
| Brand Name | AXCEL CETIRIZINE |
|---|
| Ingredients | CETIRIZINE DIHYDROCHLORIDE 10MG |
|---|
| Dosage Form | TABLET |
|---|
| Primary Packaging | ALU-PVC BLISTER |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | 10 TABS/BLIST., 10 BISTS/BOX |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | ADULT AND CHILDREN OF 3 YEARS OR ABOVE: SYMPTOMATIC TREATMENT OF SEASONAL RHINITIS, PERENNIAL ALLERGIC RHINITIS AND URTICARIA OF ALLERGIC ORIGIN |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | WHITE, LONG OBLONG SHAPED TABLET WITH SCORE LINE ON BOTH SIDES. |
|---|
| Note | |
|---|
| License Owner | VIENGTHONG PHARMA IMPORT-EXPORT SOLE CO.,LTD |
|---|
| Manufacturer | KOTRA PHARMA (M) SDN BHD |
|---|
| Country | MALAYSIA |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 07 I 3394/09 |
|---|
| FDD Registration Date | 08-APR-2024 |
|---|
| Expiry Date | 07-APR-2027 |
|---|
Back to drug list
|
