Product image of Metformin Aurobindo (Metformin Hydrochloride) supplied by GNH India

Metformin Aurobindo

Active Ingredient:
Metformin Hydrochloride
Origin:
EU

Metformin Aurobindo (Metformin Hydrochloride)

Metformin Hydrochloride, the active ingredient in Metformin Aurobindo, is a biguanide presented as an oral tablet for oral use. It is used to improve glycaemic control in adults with type 2 diabetes mellitus.

GNH India supplies Metformin Aurobindo as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Aurobindo Pharma (Malta) Limited

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Indications & Clinical Uses

Metformin Aurobindo belongs to the biguanide class and is employed in the management of disorders of glucose metabolism.

  • Type 2 diabetes mellitus: lowers fasting and post‑prandial blood glucose levels and helps achieve target HbA1c.
  • Prediabetes (impaired glucose tolerance): delays progression to overt diabetes when combined with lifestyle modification.
  • Polycystic ovary syndrome (off‑label in some regions): may improve insulin resistance and menstrual regularity.

How It Works

  • Metformin Hydrochloride decreases hepatic gluconeogenesis, reduces intestinal glucose absorption, and enhances peripheral insulin sensitivity by activating AMP‑activated protein kinase (AMPK). These actions collectively lower circulating glucose without stimulating insulin secretion, helping to control hyperglycaemia in type 2 diabetes.

Side Effects

Metformin Aurobindo may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Nausea: mild to moderate stomach upset.
  • Diarrhoea: watery stools, often early in therapy.
  • Abdominal discomfort: cramping or bloating.
  • Metallic taste: transient alteration of taste perception.
  • Decreased appetite: reduced desire to eat.
  • Vitamin B12 deficiency: long‑term use may lower levels.

Serious or Rare Side Effects

  • Lactic acidosis: rare but life‑threatening metabolic acidosis.
  • Severe hypoglycaemia: usually when combined with insulin or sulfonylureas.
  • Hepatic failure: worsening liver function may precipitate toxicity.
  • Allergic reactions: rash, pruritus, or angio‑edema.
  • Myopathy: muscle pain or weakness in rare cases.
  • Electrolyte disturbances: especially with dehydration.

Precautions & Warnings

Metformin Aurobindo requires careful patient assessment and monitoring.

  • Renal function: assess creatinine clearance before initiation and periodically thereafter.
  • Hepatic function: evaluate liver enzymes to reduce risk of lactic acidosis.
  • Cardiovascular status: avoid in patients with unstable or acute heart failure.
  • Elderly patients: start at lower doses and monitor for accumulation.
  • Concomitant alcohol use: limit intake to minimise lactic acidosis risk.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Metformin Aurobindo can interact with several medicines, altering its efficacy or safety.

Major Interactions (Avoid)

  • Iodinated contrast agents: may precipitate acute renal failure and increase lactic acidosis risk.
  • Cimetidine: can raise metformin plasma concentrations.
  • Alcohol excess: enhances risk of lactic acidosis.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask hypoglycaemia symptoms.
  • Diuretics (especially thiazides): can affect renal clearance of metformin.
  • ACE inhibitors/ARBs: monitor renal function when combined.
  • Warfarin: may require INR monitoring.
  • Antiretroviral agents (e.g., protease inhibitors): may increase metformin levels.

Frequently Asked Questions

Metformin Aurobindo is a generic formulation of metformin hydrochloride indicated for the management of type 2 diabetes mellitus. It helps lower blood glucose by improving insulin sensitivity and reducing hepatic glucose production, supporting glycaemic control in adult patients.

Metformin Hydrochloride activates AMP‑activated protein kinase (AMPK), which suppresses liver gluconeogenesis, decreases intestinal glucose absorption, and enhances peripheral tissue uptake of glucose. These combined actions lower circulating glucose without increasing insulin secretion.

The prescribed dose of Metformin Aurobindo is determined by the treating physician based on individual patient factors such as renal function, glycaemic targets, and tolerability. Dosage adjustments are made according to clinical response and safety considerations.

Metformin may be used during pregnancy when the benefits outweigh potential risks, particularly in women with pre‑existing diabetes. It is excreted in breast milk in small amounts; breastfeeding mothers should discuss continuation with their healthcare provider.

To place an order, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Metformin belongs to the biguanide class and is often first‑line therapy because it does not cause weight gain and has a low risk of hypoglycaemia compared with sulfonylureas or insulin. It can be combined with other agents for additive glucose‑lowering effects.

Metformin Aurobindo tablets should be stored at ambient temperature, below 25 °C, in the original blister pack or container. Protect them from moisture, heat and direct sunlight to maintain potency throughout the shelf‑life.

Metformin Aurobindo is taken orally, usually with meals to reduce gastrointestinal discomfort. Tablets should be swallowed whole with a glass of water; they are not intended for crushing, chewing, or dissolution unless specifically advised by a pharmacist.

The most serious risk is lactic acidosis, a rare but potentially fatal condition that can occur in patients with severe renal or hepatic impairment, acute heart failure, or excessive alcohol intake. Prompt medical attention is required if symptoms such as rapid breathing, muscle pain, or abdominal discomfort develop.

Metformin Aurobindo is contraindicated in patients with severe renal impairment (eGFR < 30 mL/min/1.73 m²), acute or chronic metabolic acidosis, known hypersensitivity to metformin, and in those with uncontrolled heart failure. Clinicians should assess each patient before initiating therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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