View drug registration information details.
| Items | Registration information |
|---|
| ID | 369 |
|---|
| No | 369 |
|---|
| Brand Name | OMEPAZ |
|---|
| Ingredients | OMEPRAZOLE SODIUM EQ. TO OMEPRAZOLE 40 MG |
|---|
| Dosage Form | POWDER FOR SOLUTION FOR INJECTION |
|---|
| Primary Packaging | VIAL |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | BOX OF 1 VIAL AND 1 AMPOULE WITH 10 ML WATER FOR INJECTION |
|---|
| Dispensing Category | |
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| ATC Classification | |
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| Pharmaceutical Class | |
|---|
| Indications | TREATMENT OF DUODENAL ULCERS, PREVENTION OF RELAPSE OF DUODENAL ULCERS, TREATMENT AND PREVENTION OF RELAPSE OF GASTRIC ULCERS, TREATMENT AND PREVENTION OF NSAID-ASSOCIATED GASTRIC AND DUODENAL ULCERS IN PATIENTS AT RISK, TREATMENT OF REFLUX OESOPHAGITIS, TREATMENT OF ZOLLINGER-ELLISON SYNDROME. |
|---|
| Contraindications | |
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| Side Effects | |
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| Unit Price | |
|---|
| EDL |
NULL |
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| Description | WHITE OR ALMOST WHITE LOOSE POWDER |
|---|
| Note | |
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| License Owner | CBF PHARMA CO.,LTD |
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| Manufacturer | CISEN PHARMACEUTICAL CO.,LTD |
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| Country | CHINA |
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| Import Registration No | |
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| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
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| Applied Date | |
|---|
| FDD Registration No | 11 I 3926/13 |
|---|
| FDD Registration Date | 14-AUG-2023 |
|---|
| Expiry Date | 13-AUG-2026 |
|---|
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