View drug registration information details.
| Items | Registration information |
|---|
| ID | 2827 |
|---|
| No | 2827 |
|---|
| Brand Name | DINAFEX 120 |
|---|
| Ingredients | FEXOFENADINE HYDROCHLORIDE USP 120 MG |
|---|
| Dosage Form | FILM-COATED TABLETS |
|---|
| Primary Packaging | ALU-PVDC BLISTER |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | BOX OF 3 X 10'S |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | RELIEF OF SYMPTOMS ASSOCIATED WITH SEASONAL ALLERGIC RHINITIS, CHRONIC IDIOPATHIC URTICARIAL AND PERENNIAL ALLERGIC RHINITIS |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | YELLOW OBLONG BICONVEX (SHALLOW) FILM COATED TABLET WITH ONE SCORE ON ONE SIDE AND PLAIN ON THE OTHER SIDE |
|---|
| Note | |
|---|
| License Owner | VIMPEX (LAO) CO.,LTD |
|---|
| Manufacturer | ESKAYEF PHARMACEUTICALS LIMITED |
|---|
| Country | BANGLADESH |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 09 I 4584/18 |
|---|
| FDD Registration Date | 07-JUL-2025 |
|---|
| Expiry Date | 06-JUL-2030 |
|---|
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