Product image of Norgesic (Orphenadrine Citrate, Paracetamol) supplied by GNH India

Norgesic

Active Ingredient:
Orphenadrine Citrate, Paracetamol
Origin:
EU

Norgesic (Orphenadrine Citrate, Paracetamol)

Orphenadrine citrate, the active ingredient in Norgesic, is a centrally acting muscle relaxant presented as an oral tablet for oral administration. In combination with paracetamol, the formulation provides analgesic and antispasmodic effects, helping to relieve muscle spasm, back pain, neck pain and other acute musculoskeletal discomfort in adult patients.

GNH India supplies Norgesic as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring quality and regulatory conformity across global markets through reliable logistics and comprehensive documentation.

Manufacturer / TM Owner

Viatris Healthcare Limited

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Indications & Clinical Uses

  • Norgesic is indicated for conditions involving skeletal muscle spasm and associated pain, acting as a combined muscle relaxant and analgesic.
  • Muscle spasm: reduction of involuntary muscle contraction and associated discomfort.
  • Acute musculoskeletal pain: relief of pain arising from soft tissue injury or strain.
  • Back pain: alleviation of low‑back muscle tension and pain.
  • Neck pain: improvement of cervical muscle stiffness and pain.

How It Works

  • Orphenadrine citrate exerts central anticholinergic activity by blocking muscarinic receptors, which diminishes skeletal muscle hyperactivity and produces relaxation. Paracetamol contributes analgesia primarily through inhibition of central cyclo‑oxygenase enzymes, reducing prostaglandin synthesis in the brain and modulating pain pathways. The combined effect provides both muscle relaxation and pain relief without significant peripheral anti‑inflammatory activity. Additionally, the formulation may enhance central analgesic pathways through serotonergic modulation.

Side Effects

Adverse reactions reported with Norgesic vary in frequency and severity.

Common Side Effects

  • Drowsiness: feeling of sleepiness or reduced alertness.
  • Dry mouth: decreased salivation causing oral discomfort.
  • Dizziness: sensation of light‑headedness or imbalance.
  • Nausea: feeling of queasiness, sometimes leading to vomiting.

Serious or Rare Side Effects

  • Severe allergic reaction: rash, swelling, or angioedema requiring immediate medical attention.
  • Hepatotoxicity: elevated liver enzymes or liver injury, especially with prolonged use.
  • Cardiac arrhythmia: irregular heart rhythm that may be life‑threatening.

Precautions & Warnings

  • Before prescribing Norgesic, clinicians should consider several safety measures.
  • Assess liver function: monitor hepatic enzymes before and during therapy.
  • Avoid in patients with known hypersensitivity to orphenadrine or paracetamol.
  • Use caution in the elderly: increased risk of sedation and falls.
  • Limit concurrent alcohol intake: may enhance hepatotoxic risk.
  • Avoid driving or operating machinery: potential drowsiness.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Norgesic may interact with other medicines; awareness of potential interactions helps ensure safe use.

Major Interactions (Avoid)

  • MAO inhibitors: risk of hypertensive crisis.
  • Other anticholinergic agents: additive anticholinergic effects.
  • Alcohol: increased sedation and hepatotoxicity.

Moderate Interactions (Monitor Closely)

  • CYP450 inhibitors (e.g., fluconazole): may raise plasma levels.
  • Anticoagulants (e.g., warfarin): possible enhancement of bleeding risk.

Frequently Asked Questions

Norgesic is prescribed to relieve muscle spasm and associated pain, including acute musculoskeletal discomfort, low‑back pain, and neck pain. It combines a central muscle relaxant with an analgesic to address both the involuntary muscle contraction and the pain that results from it.

Orphenadrine citrate acts as a central anticholinergic agent by blocking muscarinic receptors in the brain and spinal cord. This reduces skeletal muscle hyperactivity, leading to relaxation of strained muscles and decreasing the intensity of spasm‑related pain.

The dosage of Norgesic is determined by the prescribing clinician based on the patient’s condition, age, and response to therapy. The prescriber will specify the exact amount and frequency on the prescription label.

Safety data for Norgesic in pregnancy and lactation are limited. Healthcare providers should weigh the potential benefits against possible risks and consider alternative therapies when treating pregnant or nursing individuals.

To request Norgesic, submit an enquiry on the product page at gnhindia.com, indicating 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.

Norgesic combines an anticholinergic muscle relaxant (orphenadrine) with an analgesic (paracetamol), offering both spasm relief and pain control in a single tablet. Other muscle relaxants may lack an analgesic component, requiring additional medication for pain management.

Norgesic tablets should be stored at ambient temperature, preferably below 25 °C. Keep them in the original packaging, protect from moisture and direct light, and ensure they are out of reach of children.

Norgesic is taken orally as a tablet. The patient should swallow the tablet whole with water, unless otherwise directed by a healthcare professional. It is usually taken with or without food as advised by the prescriber.

Serious risks include severe allergic reactions such as rash or angioedema, liver injury (hepatotoxicity) especially with prolonged use, and cardiac arrhythmias. Patients should seek immediate medical attention if they experience any of these symptoms.

Individuals with known hypersensitivity to orphenadrine, paracetamol, or any excipients in the tablet should avoid Norgesic. It is also contraindicated in patients taking MAO inhibitors, those with severe liver disease, or anyone for whom anticholinergic effects pose a risk.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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