View drug registration information details.
| Items | Registration information |
|---|
| ID | 991 |
|---|
| No | 991 |
|---|
| Brand Name | PREDNISOLONE |
|---|
| Ingredients | PREDNISOLONE 5MG |
|---|
| Dosage Form | TABLET |
|---|
| Primary Packaging | BLISTERPACK |
|---|
| Storage | |
|---|
| Shelf Life | 4 YEARS |
|---|
| Pack Size | 10 TABS/BLIST, 10 BLISTS/BOX |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | ATOPIC DERMATITIS, INFLAMMATION AND RHEUMATIC ARTHRITIS |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | WHITE TABLET, BREAK LINE ON ONE SIDE AND OTHER SIDE MARK NO. 2 IN FOURSQUARE |
|---|
| Note | |
|---|
| License Owner | FACTORY NO.2 |
|---|
| Manufacturer | FACTORY NO. 2 |
|---|
| Country | LAO PDR |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 08 L 0139/95 |
|---|
| FDD Registration Date | 23-JUN-2025 |
|---|
| Expiry Date | 22-JUN-2030 |
|---|
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