View drug registration information details.
| Items | Registration information |
|---|
| ID | 1513 |
|---|
| No | 1513 |
|---|
| Brand Name | MANMOX -250 DRY SYRUP |
|---|
| Ingredients | AMOXICILLIN TRIHYDRATE 286.98 MG EQ.TO AMOXICILLIN 250 MG / 5 ML |
|---|
| Dosage Form | POWDER FOR ORAL SUSPENSION |
|---|
| Primary Packaging | BOTTLE |
|---|
| Storage | |
|---|
| Shelf Life | 4 YEARS |
|---|
| Pack Size | BOX OF 60 ML/BOTTLE |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | FOR THE TREATMENT OF SUSCEPTIBLE INFECTIONS INCLUDING URINARY-TRACT INFECTION, SINUSITIS, OTITIS MEDIA, UNCOMPLICATED COMMNUTY-ACQUIRED PNEUMONIA, ORAL INFECTION, LYME DISEASE, SALMONELLOSIS AND CYSTIC FIBROSIS |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | WHITE COLORED POWDER FOR ORAL SUSPENSION, AFTER RECONSTITUTION YIELDS VIOLET COLORED SUSPENSION |
|---|
| Note | |
|---|
| License Owner | LAO INTER PHARMA CO.,LTD |
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| Manufacturer | T MAN PHARMA COMPANY LIMITED |
|---|
| Country | THAILAND |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 01 I 5173/22 |
|---|
| FDD Registration Date | 21-MAY-2025 |
|---|
| Expiry Date | 20-MAY-2030 |
|---|
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