TabletsTablets
Schedule H (Prescription Required)Sulfonylureas & SecretagoguesCode: 713

Glibenclamide 5mg + Metformin Hydrochloride 500mg Tablets

Generic Formulation:Glibenclamide 5mg and Metformin Hydrochloride 500mg Tablets IP
Pack Size:10's
Common Commercial Brand Equivalents:Market reference only
Jan Aushadhi MRP
₹12.38
Brand Estimate*
₹68.14
Estimated Savings:₹55.76 (82% saved)
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*Statutory price across 21,118 listed Kendras
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Clinical Overview

Metformin Hydrochloride is the foundational first-line biguanide oral antihyperglycemic agent on the WHO Model List of Essential Medicines. It activates AMP-activated protein kinase (AMPK) in the liver, suppressing mitochondrial respiratory chain complex I, thereby potently inhibiting hepatic gluconeogenesis and glycogenolysis, while stimulating peripheral glucose uptake into skeletal muscle and delaying intestinal glucose absorption. Does not stimulate beta-cell insulin secretion, having zero intrinsic hypoglycemia risk and promoting weight neutrality or mild weight loss. Indicated as the initial pharmacological drug of choice for type 2 diabetes mellitus in adults and children aged 10 and older, and off-label in polycystic ovary syndrome (PCOS).

AI-assistedClinical summary synthesized from pharmacopoeial references (CDSCO, WHO EML, IP/BP/USP). Not clinician-reviewed. Drug code 713.Report inaccuracy

Usage Guidelines

Take orally with or immediately after meals (breakfast and dinner) with a full glass of water. Starting with a low dose (500 mg once or twice daily) and titrating slowly over weeks substantially reduces gastrointestinal side effects. Swallow sustained-release/prolonged-release tablets whole; do not break, chew, or crush.

General Administration Advice: Adhere strictly to the prescribed dosage, frequency, and treatment course. For oral medications, swallow with sufficient water. Never stop antibiotics, psychiatric medications, or antihypertensives abruptly without clinical direction.

Possible Side Effects

Common: Diarrhea, nausea, vomiting, abdominal bloating, flatulence, anorexia, metallic taste, vitamin B12 deficiency with prolonged use. Rare/Severe: Boxed warning: Lactic acidosis (rare but life-threatening accumulation with 50% mortality); acute kidney injury, and severe megaloblastic anemia.

*Note: Individual physiological responses vary. While many patients experience few or no side effects, notify your treating physician if adverse reactions persist or if hypersensitivity (angioedema, skin rash, dyspnea) occurs.

Precautions & Warnings

Black box warning: Lactic acidosis; risk is heightened in renal impairment, sepsis, acute congestive heart failure, and heavy alcohol intake. Contraindicated if eGFR < 30 mL/min; dose should not exceed 1000 mg/day if eGFR is 30-44 mL/min. Must be withheld temporarily at the time of or prior to iodinated radiocontrast imaging procedures and for 48 hours post-procedure until renal function is re-evaluated. Periodic serum vitamin B12 monitoring is advised.

Schedule H (Prescription Required)

This medication is scheduled under statutory drug regulatory frameworks (CDSCO / Drugs & Cosmetics Rules). Dispensing requires a valid medical prescription from a registered medical practitioner. Self-medication or unsupervised dosage adjustment carries significant clinical risks.

Medical Disclaimer: Statutory Clinical Disclaimer: The information provided is for educational and price-transparency purposes only and does not constitute medical advice, clinical diagnosis, or treatment recommendations. Always consult a registered endocrinologist, diabetologist, or qualified physician before initiating, adjusting dosages of, or substituting any antidiabetic or hormonal medication.