| Items | Drug Registration information |
|---|---|
| ID | 2172 |
| No | 2172 |
| Brand Name | BRUIBU SUSPENSION |
| Ingredients | IBUPROFEN BP100 MG/5 ML |
| Dosage Form | ORAL SUSPENSION |
| Primary Packaging | BOTTLE |
| Storage | |
| Shelf Life | 2 YEARS |
| Pack Size | 100 ML/BOTTLE/CARTON |
| Dispensing Category | |
| ATC Classification | |
| Pharmaceutical Class | |
| Indications | SYMPTOMATIC RELIEF OF MODERATE TO SEVERE PAIN INCLUDING HEADACHE , TOOTHACHE, BACKACHE OR PAIN ASSOCIATED WITH TRAUMA OR SURGERY. |
| Contraindications | |
| Side Effects | |
| Unit Price | |
| EDL | NULL |
| Description | ORANGE COLOURED SUSPENSION |
| 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 | 04 I 4693/19 |
| FDD Registration Date | 06/12/2022 |
| Expiry Date | 05/12/2025 |