View drug registration information details.
| Items | Registration information |
|---|
| ID | 2174 |
|---|
| No | 2174 |
|---|
| Brand Name | BRULEXIN 250 MG |
|---|
| Ingredients | CEFALEXIN MONOHYDRATE BP EQ. TO ANHYDROUS CEFALEXIN 250MG /5 ML |
|---|
| Dosage Form | POWDER FOR SUSPENSION |
|---|
| Primary Packaging | BOTTLE |
|---|
| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | 60 ML/BOTTLE/CARTON |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | RESPIRATORY TRACT INFECTION, SKIN AND SOFT TISSUE INFECTIONS, BONE AND JOINT INFECTIONS, GENITO-URINARY INFECTIONS, INCLUDING ACUTE PROSTATITIS AND DENTAL INFECTIONS. |
|---|
| Contraindications | |
|---|
| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | OFF WHITE TO LIGHT ORANGE FREE FLOWING GRANULAR POWDER FORMING ORANGE COLORED SUSPENSION ON RECONSTITUTION |
|---|
| Note | |
|---|
| License Owner | POUNSAB PHARMA CO.,LTD |
|---|
| Manufacturer | BRAWN LABORATORIES LIMITED |
|---|
| Country | INDIA |
|---|
| Import Registration No | |
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| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 01 I 4644/19 |
|---|
| FDD Registration Date | 06-DEC-2022 |
|---|
| Expiry Date | 05-DEC-2025 |
|---|
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