View drug registration information details.
| Items | Registration information |
|---|
| ID | 1793 |
|---|
| No | 1793 |
|---|
| Brand Name | LUCISETA |
|---|
| Ingredients | SPARSENTAN 200 MG |
|---|
| Dosage Form | TABLET |
|---|
| Primary Packaging | BOTTLE |
|---|
| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | BOX OF 30'S/BOTTLE |
|---|
| Dispensing Category | |
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| ATC Classification | |
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| Pharmaceutical Class | |
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| Indications | TO REDUCE PROTEINURIA IN ADULTS WITH PRIMARY IMMUNOGLOBULIN A NEPHROPATHY AT RISK OF RAPID DISEASE PROGRESSION, GENERALLY A URINE PROTEIN TO CREATININE RATIO >= 1.5 G/G |
|---|
| Contraindications | |
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| Side Effects | |
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| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | WHITE TABLET, LETTER "LUS" AND PLAIN ON THE OTHER |
|---|
| Note | |
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| License Owner | LUCIUS PHARMACEUTICALS(LAO) CO.,LTD |
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| Manufacturer | LUCIUS PHARMACEUTICALS(LAO) CO.,LTD |
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| Country | LAOS |
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| Import Registration No | |
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| Import Registration Date | |
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| Activity | CERTIFICATE RELEASED |
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| Applied Date | |
|---|
| FDD Registration No | 02 L 1302/25 |
|---|
| FDD Registration Date | 25-FEB-2025 |
|---|
| Expiry Date | 24-FEB-2030 |
|---|
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