View drug registration information details.
| Items | Registration information |
|---|
| ID | 2560 |
|---|
| No | 2560 |
|---|
| Brand Name | VEXMET 850 |
|---|
| Ingredients | Metformin Hydrochloride USP 850 mg |
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| Dosage Form | Film coated Tablets |
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| Primary Packaging | Alu-Alu Blister |
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| Storage | |
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| Shelf Life | 3 YEARS |
|---|
| Pack Size | BOX OF 10 X 10'S |
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| Dispensing Category | |
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| ATC Classification | |
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| Pharmaceutical Class | |
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| Indications | Treatment of type 2 diabetes mellitus, particularly in overweight patients, when dietary management and exercise alone does not result in adequate glycaemic control.
In adults, VEXMET may be used as monotherapy or in
combination with other oral antidiabetic agents or with insulin.
In children from 10 years of age and adolescents, VEXMET may be used as monotherapy or in combination with insulin.
A reduction of diabetic complications has been shown in
overweight type 2 diabetic adult patients treated with metformin as first-line therapy after diet failure |
|---|
| Contraindications | |
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| Side Effects | |
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| Unit Price | |
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| EDL |
NULL |
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| Description | White colour capsule shape biconvex film coated tablet. |
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| Note | |
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| License Owner | VE PRODUCTS (LAO) CO.,LTD |
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| Manufacturer | WEST-COAST PHARMACEUTICAL WORKS LTD |
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| Country | INDIA |
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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 | |
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| FDD Registration No | 12 I 5845/24 |
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| FDD Registration Date | 30-DEC-2024 |
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| Expiry Date | 29-DEC-2029 |
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