View drug registration information details.
| Items | Registration information |
|---|
| ID | 1339 |
|---|
| No | 1339 |
|---|
| Brand Name | FEXFAD TABLET 120 MG |
|---|
| Ingredients | FEXOFENADINE HYDROCHLORIDE 120 MG |
|---|
| Dosage Form | TABLET |
|---|
| Primary Packaging | ALU-ALU BLISTERPACK |
|---|
| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | 1 X 10'S/BOX |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | RELIEF OF SYMPTOMS ASSOCIATED WITH SEASONAL ALLERGIC RHINITIS IN ADULTS AND CHILDREN 12 YEARS AND OLDER |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | LASER SHINE LIGHT GREEN COLORED, ROUND, BINCONVEX, FILM COATED TABLETS |
|---|
| Note | |
|---|
| License Owner | KONGCHAI-LAO PHARMA SOLE CO.,LTD |
|---|
| Manufacturer | FOCUS & RULZ PHARMACEUTICALS (PVT) LTD |
|---|
| Country | PAKISTAN |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | STEP 1: RECEIVE (RENEW) |
|---|
| Applied Date | 29-MAY-2025 |
|---|
| FDD Registration No | 06 I 4743/19 |
|---|
| FDD Registration Date | 26-SEP-2022 |
|---|
| Expiry Date | 25-SEP-2025 |
|---|
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