View drug registration information details.
| Items | Registration information |
|---|
| ID | 2924 |
|---|
| No | 2924 |
|---|
| Brand Name | SERITO |
|---|
| Ingredients | ITOPRIDE HYDROCHLORIDE 50 MG |
|---|
| Dosage Form | TABLET |
|---|
| Primary Packaging | ALU-PVC BLISTER |
|---|
| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | BOX OF 1 X 10'S |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
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| Pharmaceutical Class | |
|---|
| Indications | FOR TREATMENT OF GASTROINTESTINAL SYMPTOMS OF FUNCTIONAL, NON ULCER DYSPEPSIA SUCH AS FEELING OF ABDIMINAL BLOATENESS, EXCESSIVE FEELING OF FULL NESS IN THE STOMACH, UPPER ABDOMINAL PAIN, DISCOMFORT, ANOREXIA, HEARTBURN, NAUSEA AND VOMITING. |
|---|
| Contraindications | |
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| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | WHITE TO ALMOST WHITE, ROUND, BICONVEX FILM COATED TABLET |
|---|
| Note | |
|---|
| License Owner | XUPTHAVYKHOUN SOLE CO.,LTD |
|---|
| Manufacturer | SERAPH PHARMACEUTICAL |
|---|
| Country | PAKISTAN |
|---|
| Import Registration No | |
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| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 02 I 5895/25 |
|---|
| FDD Registration Date | 2025-02-24 |
|---|
| Expiry Date | 2030-02-23 |
|---|
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