| ID | 450 |
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| No | 450 |
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| Brand Name | CELLCEPT 500MG |
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| Ingredients | MYCOPHENOLATE MOFETIL 500MG |
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| Dosage Form | FILM-COATED TABLETS |
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| Primary Packaging | BLISTERPACK |
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| Storage | DO NOT STORE ABOVE 25 C, STORE IN ORIGINAL CONTAINER |
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| Shelf Life | 3 YEARS |
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| Pack Size | 10'S/BLIS, 50'S, 150'S/BOX |
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| Dispensing Category | Prescription only |
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| ATC Classification | XX |
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| Pharmaceutical Class | INMUNOSUPPRESSION |
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| Indications | PROPHYLAXIS OF ACUTE ORGAN REJECTION AND FOR THE TREATMENT OF FIRST OR REFRACTORY ORGAN REJECTION IN PATIENTS RECEIVING ALLOGENEIC RENAL TRANSPLANTS; FOR THE PROPHYLAXIS OF ACUTE ORGAN REJECTION IN PATIENTS RECEIVING ALLOGENEIC CARDIAC AND HEPATIC TRANSPLANTS |
|---|
| Contraindications | HYPERSENSITIVITY TO MYCOPHENOLATE MOFETIL OR MYCOPHENOLIC ACID |
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| Side Effects | ANEMIA, NAUSEA, ABDOMINAL PAIN, SEPSIS, NAUSEA, VOMITING, DYSPEPSIA |
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| Unit Price | 100 $/50 T |
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| EDL |
No |
|---|
| Description | LAVENDER CAPLET SHAPED FILM-COATED TABLET WITH ROCHE ON ONE SIDE AND CELLCEPT 500 ON THE OTHER SIDE |
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| Note | |
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| License Owner | DKSH LAOS COMPANY LIMITED |
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| Manufacturer | DELPHARM MILANO S.R.L. |
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| Country | ITALY |
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| Import Registration No | 53338 01 |
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| Import Registration Date | 2013-06-09 |
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| Activity | CERTIFICATE RELEASED |
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| Applied Date | 2021-09-06 |
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| FDD Registration No | 07 I 2309/04 |
|---|
| FDD Registration Date | 2022-07-22 |
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| Expiry Date | 2025-07-21 |
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