View drug registration information details.
| Items | Registration information |
|---|
| ID | 982 |
|---|
| No | 982 |
|---|
| Brand Name | PHOPRETO |
|---|
| Ingredients | PRETOMANID 200 MG |
|---|
| Dosage Form | TABLET |
|---|
| Primary Packaging | BOTTLE |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | BOX OF 120 TABLETS/BOTTLE |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | AS PART OF COMBINATION REGIMEMN WITH BEDAQUILINE AND LINEZOLID FOR THE TREATMENT OF ADULT WITH PULMONARY EXTENSIVELY DRUG RESISTANT |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | WHITE BICONVEX TABLET |
|---|
| 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 | 05 L 0976/23 |
|---|
| FDD Registration Date | 17-MAY-2023 |
|---|
| Expiry Date | 16-MAY-2026 |
|---|
Back to drug list
|
