| ID | 591 |
|---|
| No | 591 |
|---|
| Brand Name | RECORMON 4,000 IU |
|---|
| Ingredients | EPOETIN BETA 4,000 IU/0.3ML |
|---|
| Dosage Form | SOLUTION FOR INJECTION |
|---|
| Primary Packaging | syringe |
|---|
| Storage | STORE AT 2C-8C |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | BOX OF 6 PRE-FILLED SYRINGES WITH NEEDLES 27 G1/12 |
|---|
| Dispensing Category | Prescription only |
|---|
| ATC Classification | B03XA01 |
|---|
| Pharmaceutical Class | ANTIANEMICS/PRE & POST NATAL VITAMINS |
|---|
| Indications | TREATMENT OF: RENAL ANEMIA, SYMPTOMATIC ANEMIA IN CANCER PATIENTS. - PREVENTION OF ANEMIA OF PREMATURITY. - TREATMENT FOR INCREASING THE AMOUNT OF AUTOLOGOUS BLOOD |
|---|
| Contraindications | POOLY CONTROLLED HYPERSENSITIVITY TO THE ACTIVE SUBSTANCE OR TO ANY OF EXCIPIENTS OF THE PRODUCT |
|---|
| Side Effects | INCREASE IN BLOOD PRESSURE HEADACHE, SHUNT THEROMBOSIS, THROMBOCYTOSIS |
|---|
| Unit Price | - |
|---|
| EDL |
No |
|---|
| Description | COLOURLESS, CLEAR SOLUTION |
|---|
| Note | |
|---|
| License Owner | DKSH LAOS COMPANY LIMITED |
|---|
| Manufacturer | ROCHE DIAGNOSTICS GMBH |
|---|
| Country | GERMANY |
|---|
| Import Registration No | 54766 08 |
|---|
| Import Registration Date | 2013-02-07 |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | 2022-12-09 |
|---|
| FDD Registration No | 09 I 2082/01 |
|---|
| FDD Registration Date | 2023-03-31 |
|---|
| Expiry Date | 2026-03-30 |
|---|
