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

Metformin Hydrochloride Sandoz

Active Ingredient:
Metformin Hydrochloride
Origin:
EU

Metformin Hydrochloride Sandoz (Metformin Hydrochloride)

Metformin Hydrochloride, the active ingredient in Metformin Hydrochloride Sandoz, is a biguanide presented as an oral tablet for oral use. It is used to improve blood glucose control in adults with type 2 diabetes mellitus.
GNH India supplies Metformin Hydrochloride Sandoz as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Sandoz Gmbh

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Indications & Clinical Uses

Metformin Hydrochloride is indicated for conditions affecting glucose metabolism and insulin sensitivity.

  • Type 2 diabetes mellitus: lowers fasting and post‑prandial blood glucose levels to achieve glycaemic targets.
  • Prediabetes: helps delay progression to overt diabetes by improving insulin sensitivity.
  • 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‑mediated glucose uptake. By activating AMP‑activated protein kinase (AMPK), it modulates cellular energy balance, leading to lowered circulating glucose without stimulating insulin secretion.

Side Effects

Metformin Hydrochloride may cause a range of adverse reactions.

Common Side Effects

  • Nausea: mild to moderate stomach upset, often transient.
  • Diarrhoea: loose stools, usually early in therapy.
  • Abdominal discomfort: cramping or bloating.
  • Metallic taste: transient alteration in taste perception.
  • Loss of appetite: reduced desire to eat.
  • Flatulence: increased intestinal gas.

Serious or Rare Side Effects

  • Lactic acidosis: rare but life‑threatening metabolic disturbance.
  • Severe skin reactions: such as Stevens‑Johnson syndrome.
  • Hepatic dysfunction: signs of liver injury.
  • Significant hypoglycaemia: when combined with other glucose‑lowering agents.
  • Vitamin B12 deficiency: may develop with long‑term use.
  • Acute pancreatitis: rare inflammatory condition of the pancreas.

Precautions & Warnings

Metformin Hydrochloride requires careful patient assessment and monitoring.

  • Renal function: evaluate creatinine clearance before initiation and periodically thereafter.
  • Hepatic function: avoid use in patients with severe liver disease.
  • Risk of lactic acidosis: contraindicated in severe renal impairment or acute metabolic acidosis.
  • Pregnancy: use only if potential benefit justifies potential risk to the fetus.
  • Alcohol consumption: limit intake to reduce risk of acidosis.
  • Store at ambient temperature: keep in the original container, protect from moisture and heat.

Avoid Interactions

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

Major Interactions (Avoid)

  • Iodinated contrast media: may precipitate renal dysfunction and lactic acidosis.
  • Cimetidine: can increase metformin plasma concentrations.
  • Alcohol: potentiates risk of lactic acidosis.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask hypoglycaemic symptoms.
  • Diuretics: can affect renal clearance of metformin.

Frequently Asked Questions

Metformin Hydrochloride Sandoz is an oral biguanide indicated for the management of type 2 diabetes mellitus. It helps lower elevated blood glucose levels by improving insulin sensitivity and reducing hepatic glucose production.

The drug activates AMP‑activated protein kinase (AMPK), which suppresses liver glucose output, decreases intestinal glucose absorption, and enhances peripheral uptake of glucose into muscle cells, thereby improving overall glycaemic control without increasing insulin secretion.

The appropriate dose is determined by the prescribing clinician based on the individual’s medical condition, renal function, and response to therapy. Dosage adjustments are made according to clinical judgement and patient tolerance.

Metformin may be used during pregnancy only if the potential benefit outweighs the possible risk to the fetus, and it is generally considered compatible with breastfeeding, though the prescriber should evaluate each case individually.

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 is the first‑line therapy for type 2 diabetes due to its efficacy, low risk of hypoglycaemia and favourable impact on weight. Unlike sulfonylureas or insulin, it does not stimulate insulin release, making it a preferred option for many patients.

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

The medication is taken orally, usually with meals to reduce gastrointestinal discomfort. Tablets should be swallowed whole with a full glass of water and not crushed or chewed unless otherwise directed by a healthcare professional.

The most critical adverse effect is lactic acidosis, a rare but potentially fatal condition, especially in patients with severe renal impairment, hepatic disease, or excessive alcohol intake. Prompt medical attention is required if symptoms such as rapid breathing, muscle pain or abdominal discomfort occur.

Patients with severe renal impairment (eGFR < 30 mL/min/1.73 m²), acute or chronic metabolic acidosis, known hypersensitivity to metformin, or those receiving iodinated contrast agents for imaging should avoid using this medication.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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