View drug registration information details.
| Items | Registration information |
|---|
| ID | 1581 |
|---|
| No | 1581 |
|---|
| Brand Name | RILAST 500 |
|---|
| Ingredients | RITUXIMAB (R-DNA ORIGIN) 500 MG/ 50 ML |
|---|
| Dosage Form | SOLUTION FOR INJECTION |
|---|
| Primary Packaging | VIAL |
|---|
| Storage | |
|---|
| Shelf Life | 30 MONTHS |
|---|
| Pack Size | BOX OF 1 VIAL X 50 ML |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | NON HODGKIN'S LYMPHOMA, PATIENTS WITH DIAGNOSED CHRONIC LYMPHOCYTIC LEUKEMIA, RHEUMATOID ARTHRITIS, GRANULOMATOSIS WITH POLYANGIITIS AND MICROSCOPIC POLYANGITIS |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | STERILE, CLEAR, COLORLESS SOLUTION |
|---|
| Note | |
|---|
| License Owner | LAO NIYOM PHARMA SOLE CO.,LTD |
|---|
| Manufacturer | HETERO BIOPHARMA LIMITED |
|---|
| Country | INDIA |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 12 I 5366/22 |
|---|
| FDD Registration Date | 30-DEC-2022 |
|---|
| Expiry Date | 29-DEC-2025 |
|---|
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