| ID | 521 |
|---|
| No | 521 |
|---|
| Brand Name | LODOZ 2.5 MG/ 6.25 MG |
|---|
| Ingredients | BISOPROLOL FUMARATE 2.50 MG, HYDROCHLOROTHIAZIDE 6.25 MG |
|---|
| Dosage Form | FILM COATED TABLET |
|---|
| Primary Packaging | ALU-ALU BLISTER |
|---|
| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | BOX OF 30 TABLETS |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | MILD TO MODERATE ESSENTIAL HYPERTENSION |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL | NULL |
|---|
| Description | YELLOW, ROUND, BICONVEX UPPER SIDE EMBOSSED HEART, DOWNSIDE EMBOSSED 2.5 |
|---|
| Note | |
|---|
| License Owner | DKSH LAOS COMPANY LIMITED |
|---|
| Manufacturer | MERCK HEALTHCARE KGaA |
|---|
| Country | FRANCE |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 12 I 5012/20 |
|---|
| FDD Registration Date | 08/04/2024 |
|---|
| Expiry Date | 07/04/2027 |
|---|
