| ID | 1635 |
|---|
| No | 1635 |
|---|
| Brand Name | BEDAQUIS |
|---|
| Ingredients | BEDAQUILLINE FUMARATE 100 MG |
|---|
| Dosage Form | TABLET |
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| Primary Packaging | BOTTLE |
|---|
| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | 188 TABLESTS/BOTTLE |
|---|
| Dispensing Category | |
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| ATC Classification | |
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| Pharmaceutical Class | |
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| Indications | AS PART OF COMBINATION THERAPY IN ADULTS (>= 18 YEARS) WITH PULMONARY MULTI-DRUG-REISITANT TUBERCULOSIS (MDR-TB) |
|---|
| Contraindications | |
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| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | WHITE TABLETS |
|---|
| Note | |
|---|
| License Owner | LAOS ALLIANCE PHARMACEUTICAL GROUP COMPANY |
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| Manufacturer | LAOS ALLIANCE PHARMACEUTICAL GROUP COMPANY |
|---|
| Country | LAOS |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 03 L 1310/25 |
|---|
| FDD Registration Date | 31-MAR-2025 |
|---|
| Expiry Date | 30-MAR-2030 |
|---|
