View drug registration information details.
| Items | Registration information |
|---|
| ID | 2540 |
|---|
| No | 2540 |
|---|
| Brand Name | PREDNIVEX 4 |
|---|
| Ingredients | METHYLPREDNISOLONE USP 4 MG |
|---|
| Dosage Form | TABLET |
|---|
| Primary Packaging | ALU-ALU BLISTER |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | BOX OF 3 X 10'S |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | PRIMARY AND SECONDARY ADRENAL INSUFFICIENCY, CONGENITAL ADRENAL HYPERPLASIA, RHEUMATOID ARTHRITIS, JUVENILE CHRONIC ARTHRITIS, ANKYLOSING SPONDYLITIS, SYSTEMIC LUPUS ERYTHEMATOSUS, RHEUMATIC FEVER WITH SEVERE CARDITIS, ALLERGIC STATE, PEMPHIGUS VULGARIS, OPTIC NEURITIS, PULMONARY SARCOID |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | WHITE COLOR ROUND SHAPED FLAT UNCOATED TABLET WITH BREAKLINE ON ONE SIDE |
|---|
| Note | |
|---|
| License Owner | VE PRODUCTS (LAO) CO.,LTD |
|---|
| Manufacturer | WEST-COAST PHARMACEUTICAL WORKS LTD. |
|---|
| Country | INDIA |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 09 I 5152/21 |
|---|
| FDD Registration Date | 25-SEP-2024 |
|---|
| Expiry Date | 24-SEP-2029 |
|---|
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