View drug registration information details.
| Items | Registration information |
|---|
| ID | 2171 |
|---|
| No | 2171 |
|---|
| Brand Name | BRUIBU 400 |
|---|
| Ingredients | IBUPROFEN BP 400 MG |
|---|
| Dosage Form | FILM COATED TABLET |
|---|
| Primary Packaging | ALU-PVC BLISTERPACK |
|---|
| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | 10 X 10'S/CARTON |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | RHEUMATIC OR MUSCULAR PAIN, BACKACHE, NEURALGIA, MIGRAINE, HEADACHE, DENTAL PAIN, DYSMENORRHOEA, FEVERISHNESS, SYMPTOMS OF COLD AND INFLUENZA |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | PINK COLORED, ROUND, BICONVEX, FILM COATED TABLET |
|---|
| Note | |
|---|
| License Owner | POUNSAB PHARMA CO.,LTD |
|---|
| Manufacturer | BRAWN LABORATORIES LIMITED |
|---|
| Country | INDIA |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 01 I 4649/19 |
|---|
| FDD Registration Date | 06-DEC-2022 |
|---|
| Expiry Date | 05-DEC-2025 |
|---|
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