View drug registration information details.
| Items | Registration information |
|---|
| ID | 491 |
|---|
| No | 491 |
|---|
| Brand Name | GAVISCON SUSPENSION |
|---|
| Ingredients | SODIUM ALGINATE 500 MG, SODIUM BICARBONATE 267 MG, CALCIUM CARBONATE 160 MG |
|---|
| Dosage Form | SUSPENSION |
|---|
| Primary Packaging | SACHET |
|---|
| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | BOX OF 12 SACHETS X 10ML |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
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| Pharmaceutical Class | |
|---|
| Indications | TREATMENT OF SYMPTOMS OF GASTRO-OESOPHAGEAL REFLUX SUCH AS ACID REGURGITATION, HEARTBURN AND INDIGESTION RELATED TO REFLUX, FOR EXAMPLE, FOLLOWING MEALS, OR DURING PREGNANCY, OR IN PATIENTS WITH SYMPTOMS RELATED TO REFLUX OESOPHAGITIS |
|---|
| Contraindications | |
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| Side Effects | |
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| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | AN OFF WHITE SUSPENSION WITH ODOUR AND FLAVOUR OF PEPERMINT |
|---|
| Note | |
|---|
| License Owner | DKSH LAOS COMPANY LIMITED |
|---|
| Manufacturer | RECKITT BENCKISER HEALTHCARE(UK)LIMITED |
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| Country | UNITED KINGDOM |
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| Import Registration No | |
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| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 01 I 5373/23 |
|---|
| FDD Registration Date | 23-Jan-2023 |
|---|
| Expiry Date | 22-Jan-2026 |
|---|
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