View drug registration information details.
| Items | Registration information |
|---|
| ID | 2060 |
|---|
| No | 2060 |
|---|
| Brand Name | FENAFEX 180 MG |
|---|
| Ingredients | FEXOFENADINE HYDROCHLORIDE 180 MG |
|---|
| Dosage Form | FILM-COATED TABLETS |
|---|
| Primary Packaging | ALU-ALU BLISTER |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | 10 TABLETS/BLISTER, 1 BLISTER/BOX, 10 BLISTERS/BOX |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | FOR THE RELIEF OF SYMPTOMS ASSOCIATED WITH ALLERGIC RHINITIS AND CHRONIC IDIOPATHIC URTICARIA IN ADULTS AND CHILDREN 12 YEARS OF AGE AND OLDER |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | ORANGE OBLONG BICONVEX FILM COATED TABLET EMBOSSED WITH '' SO8'' ON ONE SIDE AND A BREAK LINE ON THE OTHER SIDE. |
|---|
| Note | |
|---|
| License Owner | PALAMY PHARMA CO., LTD |
|---|
| Manufacturer | SRIPRASIT PHARMA CO., LTD |
|---|
| Country | THAILAND |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 03 I 3778/12 |
|---|
| FDD Registration Date | 19-MAY-2023 |
|---|
| Expiry Date | 18-MAY-2026 |
|---|
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