View drug registration information details.
| Items | Registration information |
|---|
| ID | 1473 |
|---|
| No | 1473 |
|---|
| Brand Name | DICLOXA RX 500 |
|---|
| Ingredients | DICLOXACILLIN SODIUM 566 MG EQ. TO DICLOXACILLIN 500 MG |
|---|
| Dosage Form | CAPSULE |
|---|
| Primary Packaging | ALU-PVC |
|---|
| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | BOX OF 25 X 10'S |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | SHARE THE USES OF OTHER PENICILLINASE-RESISTANT PENICILLINS AND GENERALLY IS USED ONLY IN THE TREATMENT OF INFECTIONS CAUSED BY, OR SUSPECTED OF BEING CAUSED BY SUSCEPTIBLE PENICILLINASE -RESISTANT STAPHYLOCOCCI |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | BLUE-WHITE CAPSULE CONTAINING WHITE TO YELLOWISH WHITE GRANULAR POWDER |
|---|
| Note | |
|---|
| License Owner | LAO INTER PHARMA CO.,LTD |
|---|
| Manufacturer | R X MANUFACTURING CO.,LTD |
|---|
| Country | THAILAND |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 05 I 5106/21 |
|---|
| FDD Registration Date | 07-FEB-2025 |
|---|
| Expiry Date | 06-FEB-2030 |
|---|
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