View drug registration information details.
| Items | Registration information |
|---|
| ID | 2094 |
|---|
| No | 2094 |
|---|
| Brand Name | OMENIX 40 |
|---|
| Ingredients | OMEPRAZOLE SODIUM BP 44.6323 MG EQ. TO OMEPRAZOLE 40 MG |
|---|
| Dosage Form | POWDER FOR SOLUTION FOR INJECTION |
|---|
| Primary Packaging | VIAL |
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| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | BOX OF 1 VIAL + 1 AMPOULE OF 10 ML WATER FOR INJECTIONON |
|---|
| Dispensing Category | |
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| ATC Classification | |
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| Pharmaceutical Class | |
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| Indications | HEARTBURN, ANY SYMPTOMS OF GERD, EROSIVE ESOPHAGITIS, GASTRIC ULCER, DUODENAL ULCER AND REDUCTION OF RISK OF UPPER GI BLEEDING IN CRITICALLY ILL PATIENTS, PRIMARILY FOR THE TREATMENT OF ZOLLINGER-ELLISON SYNDROME |
|---|
| Contraindications | |
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| Side Effects | |
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| Unit Price | |
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| EDL |
NULL |
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| Description | STERILE, FREEZE-DRIED, WHITE TO OFF-WHITE POROUS CAKE OR POWDER FILLED IN COLORLESS GLASS VIAL.
THE RECONSTITUTED SOLUTION IS CLEAR, COLORLESS AND HAVING NO VISIBLE RESIDUE AS UNDISSOLVED MATTER
|
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| Note | |
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| License Owner | PALAMY PHARMA CO., LTD |
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| Manufacturer | INCEPTA PHARMACEUTICALS LIMITED |
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| Country | BANGLADESH |
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| Import Registration No | |
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| Import Registration Date | |
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| Activity | CERTIFICATE RELEASED |
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| Applied Date | |
|---|
| FDD Registration No | 05 I 3321/09 |
|---|
| FDD Registration Date | 23-NOV-2023 |
|---|
| Expiry Date | 22-Nov-2026 |
|---|
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