View drug registration information details.
| Items | Registration information |
|---|
| ID | 1551 |
|---|
| No | 1551 |
|---|
| Brand Name | TREVIA TABLETS 100 MG |
|---|
| Ingredients | SITAGLIPTIN PHOSPHATE MONOHYDRATE EQ.TO SITAGLIPTIN 100 MG |
|---|
| Dosage Form | FILM-COATED TABLETS |
|---|
| Primary Packaging | ALU-ALU |
|---|
| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | BOX OF 5 X 7'S AND BOX OF 2 X 7'S |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | TREVIA ( SITAGLITIN) IS INDICATED IN PATIENTS WITH TYPE 2 DIABETES MELLITUS AS AN ADJUNCT KTO DIET AND EXERCISE TO IMPROVE GLYCEMIC CONTROL. |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | PEACH ORANGE COLORED, ROUND SHAPED BICONVEX, FILM- COATED TABLET, BISECT LINE ON ONE SIDE AND PLAIN ON THER SIDE. |
|---|
| Note | |
|---|
| License Owner | LAO INTER PHARMA CO.,LTD |
|---|
| Manufacturer | GETZ PHARMA (PRIVATE) LIMITED |
|---|
| Country | PAKISTAN |
|---|
| Import Registration No | |
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| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 11 I 4110/15 |
|---|
| FDD Registration Date | 19-Apr-2023 |
|---|
| Expiry Date | 18-Apr-2026 |
|---|
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