Human Formulations

Glimepiride 2mg + Metformin Hcl (Prolonged Released) 1000mg Tablets IP (Uncoated Bilayered)

Glimepiride 2mg + Metformin Hcl (Prolonged Released) 1000mg Tablets IP (Uncoated Bilayered) is a bilayered tablet formulated with Glimepiride 2mg + Metformin Hcl (Prolonged Released) 1000mg IP ( ). The listed active ingredient profile is Glimepiride; Metf

Therapeutic RangesDiabetic Range Single Ingredient Bilayered Tablet
Sterile injectable formulation

Product information

Product Line
Human Formulations
Category
Therapeutic Ranges, Diabetic Range
Dosage Form
Bilayered Tablet
Product Type
Single Ingredient

Available strengths

Glimepiride 2mg + Metformin Hcl (Prolonged Released) 1000mg IP ( )

Description

Glimepiride 2mg + Metformin Hcl (Prolonged Released) 1000mg Tablets IP (Uncoated Bilayered) is a bilayered tablet formulated with Glimepiride 2mg + Metformin Hcl (Prolonged Released) 1000mg IP ( ). The listed active ingredient profile is Glimepiride; Metformin Hcl, placing the product in the oral antidiabetic category. The formulation contains one or more oral glucose-lowering medicines used in clinician-directed management of type 2 diabetes mellitus. The source indicates prolonged release; uncoated; bilayered characteristics, which should be retained exactly because release technology can affect administration and product performance. For website cataloguing, the composition, strength, dosage form and formulation characteristics should be displayed prominently and consistently. The product description should remain factual and should not include unapproved cure, superiority, guaranteed-result or broad therapeutic claims. Clinical selection should depend on diagnosis, patient-specific factors, contraindications, concomitant medicines and professional judgement. Prescription status, warnings, interactions, adverse effects and dosing or application instructions must be checked against the current approved product label. Manufacturer, licence, storage, shelf-life, reconstitution where applicable, and market-specific regulatory details should be added only from verified product documentation.
WHO-GMP Sourced
Sterile Supply
Regulatory Documentation
Quality Assured