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

Moxifloxacin Hydrochloride Aurobindo

Active Ingredient:
Moxifloxacin Hydrochloride
Origin:
EU

Moxifloxacin Hydrochloride Aurobindo (Moxifloxacin Hydrochloride)

Moxifloxacin Hydrochloride, the active ingredient in Moxifloxacin Hydrochloride Aurobindo, is a fluoroquinolone antibiotic presented as an oral dosage form for systemic use. It treats a range of serious bacterial infections, particularly in adult patients with community‑acquired pneumonia, acute bacterial sinusitis, acute exacerbations of chronic bronchitis, and skin and skin‑structure infections.

GNH India supplies Moxifloxacin Hydrochloride Aurobindo as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable logistics for global distribution.

Manufacturer / TM Owner

Aurobindo Pharma B.V.

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Indications & Clinical Uses

Moxifloxacin Hydrochloride is indicated for several bacterial infections affecting the respiratory tract and skin.

  • Community‑acquired bacterial pneumonia: reduces bacterial load and improves clinical outcomes in adult patients.
  • Acute bacterial sinusitis: eradicates causative pathogens and relieves sinus inflammation.
  • Acute bacterial exacerbation of chronic bronchitis: treats infection-driven worsening of chronic bronchitis symptoms.
  • Skin and skin structure infections: combats susceptible Gram‑positive and Gram‑negative bacteria in skin lesions.

How It Works

  • Moxifloxacin Hydrochloride exerts its antibacterial effect by binding to bacterial DNA gyrase (topoisomerase II) and topoisomerase IV. Inhibition of these enzymes prevents the supercoiling and relaxation of DNA that are essential for replication and transcription, leading to bacterial cell death. The dual targeting of both enzymes enhances activity against a broad spectrum of Gram‑positive and Gram‑negative organisms, including many resistant strains.

Side Effects

Moxifloxacin Hydrochloride may cause adverse reactions, which are classified by frequency and severity.

Common Side Effects

  • Nausea: mild gastrointestinal upset occurring in many patients.
  • Diarrhea: loose stools that are usually self‑limiting.
  • Headache: transient cranial pain reported during therapy.

Serious or Rare Side Effects

  • Tendon rupture: rare but severe injury to tendons, especially the Achilles.
  • QT interval prolongation: potential cardiac rhythm disturbance requiring monitoring.
  • Severe allergic reaction: anaphylaxis or angioedema requiring immediate medical attention.

Precautions & Warnings

Before prescribing Moxifloxacin Hydrochloride, clinicians should consider several precautionary measures to ensure safe use.

  • Assess renal function: dose adjustment may be needed in patients with impaired clearance.
  • Review cardiac history: avoid use in individuals with known QT prolongation or arrhythmias.
  • Evaluate tendon health: discontinue if patient reports tendon pain or swelling.
  • Avoid concomitant use with drugs that prolong QT: monitor for additive cardiac effects.
  • Store at ambient temperature: keep below 25 °C in the original container, protected from moisture and light.

Avoid Interactions

Moxifloxacin Hydrochloride can interact with other medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • Antacids containing aluminum or magnesium: reduce absorption of the antibiotic.
  • Warfarin: may increase anticoagulant effect and bleeding risk.
  • Cyclosporine: can raise cyclosporine concentrations leading to toxicity.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may increase risk of central nervous system stimulation.
  • Theophylline: potential for elevated serum levels and side effects.
  • Corticosteroids: combined use may heighten risk of tendon rupture.

Frequently Asked Questions

Moxifloxacin Hydrochloride is a prescription fluoroquinolone antibiotic used to treat adult patients with community‑acquired bacterial pneumonia, acute bacterial sinusitis, acute bacterial exacerbations of chronic bronchitis, and skin or skin‑structure infections caused by susceptible bacteria.

The drug inhibits bacterial DNA gyrase (topoisomerase II) and topoisomerase IV, enzymes essential for DNA replication and transcription. By blocking these targets, it prevents bacterial cell division and leads to rapid bacterial death across a broad spectrum of Gram‑positive and Gram‑negative organisms.

The specific dose and treatment duration are determined by the prescribing clinician based on the infection type, severity, patient age, renal function, and other clinical factors. No fixed dosing information is provided here; the prescriber sets the appropriate regimen.

Safety data for Moxifloxacin in pregnancy and lactation are limited. The drug should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and it is generally avoided unless no suitable alternatives exist.

Enquiries are submitted via the product page on gnhindia.com, where you specify 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.

Moxifloxacin offers a broader spectrum against both Gram‑positive and Gram‑negative bacteria and has enhanced activity against atypical pathogens compared with older fluoroquinolones such as ciprofloxacin. It also has a longer half‑life, allowing once‑daily dosing, but shares class‑related safety considerations.

Store the product at ambient temperature, preferably below 25 °C, in its original packaging. Protect it from moisture, direct sunlight and extreme heat. Keep the container tightly closed and out of reach of children.

Moxifloxacin Hydrochloride is administered orally, usually as a tablet. It can be taken with or without food, but consistent intake with respect to meals helps maintain stable absorption. Swallow the tablet whole with water; do not crush or chew unless directed by a healthcare professional.

Serious adverse events include tendon rupture (especially the Achilles tendon), QT interval prolongation that may lead to arrhythmias, and severe hypersensitivity reactions such as anaphylaxis or angioedema. Patients should seek immediate medical attention if they experience sudden tendon pain, palpitations, or signs of an allergic reaction.

Moxifloxacin is contraindicated in patients with a known hypersensitivity to the drug or any fluoroquinolone, those with a history of tendon disorders related to fluoroquinolone use, and individuals with established prolonged QT interval or uncontrolled cardiac arrhythmias. Caution is also advised for patients with severe renal impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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