View drug registration information details.
| Items | Registration information |
|---|
| ID | 2861 |
|---|
| No | 2861 |
|---|
| Brand Name | NEOSALINE |
|---|
| Ingredients | SODIUM CHLORIDE BP 1.300G, POTASSIUM CHLORIDE BP 0.750G, SODIUM CITRATE BP 1.450G, ANHYDROUS GLUCOSE BP 6.750 G |
|---|
| Dosage Form | POWDER FOR ORAL SOLUTION |
|---|
| Primary Packaging | SACHET |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | BOX OF 50 SACHETS |
|---|
| Dispensing Category | |
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| ATC Classification | |
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| Pharmaceutical Class | |
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| Indications | REPLACEMENT OF FLUID AND ELECTROLYTE LOSS DUE TO ACUTE DIARRHEA, VOMITING & DEHYDRATION, OTHER CONDITIONS OF FLUID LOSS OR LACK OF INTAKE IN PATIENTS OF ALL AGE GROUPS. |
|---|
| Contraindications | |
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| Side Effects | |
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| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | WHITE CRYSTALLINE, FREE FLOWING POWDER |
|---|
| Note | |
|---|
| License Owner | VIMPEX (LAO) CO.,LTD |
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| Manufacturer | ESKAYEF PHARMACEUTICALS LIMITED |
|---|
| Country | BANGLADESH |
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| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 09 I 4584/18 |
|---|
| FDD Registration Date | 07-JUL-2025 |
|---|
| Expiry Date | 06-JUL-2030 |
|---|
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