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 indicated for the management of type 2 diabetes mellitus and related glucose‑handling disorders in adult patients.
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 used to improve glycaemic control in disorders of glucose metabolism.

  • Type 2 diabetes mellitus: lowers fasting and post‑prandial blood glucose levels.
  • Prediabetes (impaired glucose tolerance): delays progression to overt diabetes.
  • Polycystic ovary syndrome: reduces insulin resistance and may improve menstrual regularity.

How It Works

  • Metformin Hydrochloride reduces hepatic gluconeogenesis, decreases 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 maintain stable blood‑sugar levels in patients with insulin resistance.

Side Effects

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

Common Side Effects

  • Gastrointestinal upset: nausea, abdominal discomfort, or loss of appetite.
  • Diarrhea: frequent loose stools, especially during treatment initiation.
  • Metallic taste: transient alteration in taste perception.
  • Flatulence: increased intestinal gas.
  • Weight loss: modest reduction in body weight.

Serious or Rare Side Effects

  • Lactic acidosis: a rare but life‑threatening accumulation of lactate.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hepatotoxicity: abnormal liver enzymes indicating liver injury.
  • Vitamin B12 deficiency: may develop with long‑term therapy.
  • Hypoglycaemia: uncommon when used alone but possible with other glucose‑lowering agents.

Precautions & Warnings

Before initiating Metformin Aurobindo, clinicians should evaluate patient‑specific risk factors and monitor relevant parameters.

  • Renal function: assess creatinine clearance and avoid use in severe renal impairment.
  • Hepatic function: check liver enzymes; avoid in active liver disease.
  • Risk of lactic acidosis: consider comorbidities such as heart failure, hypoxia, or sepsis.
  • Elderly patients: start at lower doses and monitor tolerance closely.
  • Vitamin B12 status: periodic testing is advisable during prolonged therapy.
  • Store at room temperature: keep in the original container, protect from moisture and heat.

Avoid Interactions

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

Major Interactions (Avoid)

  • Iodinated contrast agents: may precipitate acute renal failure and increase lactic acidosis risk.
  • Cimetidine: can raise metformin plasma concentrations.
  • Alcohol (excessive): enhances risk of lactic acidosis.
  • Diuretics (e.g., thiazides): may impair renal clearance of metformin.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask hypoglycaemia symptoms.
  • ACE inhibitors or ARBs: monitor renal function when combined.
  • Other antidiabetic agents (e.g., sulfonylureas): increase risk of hypoglycaemia.
  • CYP450 inhibitors (e.g., trimethoprim): may affect renal handling of metformin.

Frequently Asked Questions

Metformin Aurobindo is an oral biguanide indicated for the treatment of type 2 diabetes mellitus. It helps lower fasting and post‑prandial blood glucose by improving the body’s response to insulin and reducing hepatic glucose production.

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

The dosage of Metformin Aurobindo is individualized by the prescribing clinician based on the patient’s glycaemic targets, renal function, and tolerability. The prescriber determines the appropriate strength, frequency, and titration schedule.

Metformin Aurobindo is classified as Pregnancy Category B, indicating that animal studies have not shown risk and there are no well‑controlled human studies. It may be used during pregnancy when benefits outweigh potential risks, and it is excreted in breast milk in small amounts; clinicians should weigh the advantages and discuss with the patient.

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 (including any cold‑chain requirements), and necessary import documentation.

Compared with sulfonylureas, metformin does not stimulate insulin release, so it carries a lower risk of hypoglycaemia. Unlike insulin, it is taken orally and does not require injection. Its primary advantage is improving insulin sensitivity and having a neutral or modest weight‑loss effect, making it a first‑line therapy for many patients with type 2 diabetes.

Metformin Aurobindo tablets should be stored at room temperature, below 25 °C, in the original packaging to protect from moisture and light. Keep the container tightly closed and out of reach of children.

Metformin Aurobindo is taken orally, usually with meals to reduce gastrointestinal discomfort. The tablets are swallowed whole with a glass of water; they should not be crushed or chewed unless specifically instructed by a healthcare professional.

The most serious risk is lactic acidosis, a rare but potentially fatal condition that can occur in patients with severe renal impairment, hepatic disease, or conditions causing hypoxia. Prompt medical attention is required if symptoms such as unexplained fatigue, muscle pain, breathing difficulty, 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, including diabetic ketoacidosis, and in those with known hypersensitivity to metformin or any component of the formulation.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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