GNH USA

Europe — EMA

Libroxar

GNH USA supplies Libroxar (Buprenorphine/Naloxone), a partial opioid agonist/antagonist for opioid dependence and opioid use disorder.

Buprenorphine, Naloxone

Request sourcing

1
Pack/s

What is Buprenorphine, Naloxone?

Buprenorphine/Naloxone, the active ingredient in Libroxar, is a Partial opioid agonist / opioid antagonist combination presented as a sublingual formulation for sublingual use. It treats opioid dependence and opioid use disorder in adults.

GNH USA supplies Libroxar as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Buprenorphine, Naloxone used for?

Libroxar is used in the management of opioid dependence and related disorders, acting on the opioid receptor system to reduce withdrawal and cravings.

- Opioid dependence: helps maintain abstinence by reducing withdrawal symptoms and cravings. - Opioid use disorder: supports long‑term recovery and stabilisation in patients with opioid misuse. - Relapse prevention: lowers the risk of relapse by providing a controlled opioid effect while blocking full agonist activity.

What are the side effects of Buprenorphine, Naloxone?

Common Side Effects: - Nausea: mild to moderate stomach upset. - Constipation: reduced bowel movements. - Headache: transient cranial pain. - Sweating: increased perspiration, especially at night. - Insomnia: difficulty falling or staying asleep. - Dry mouth: reduced salivation.

Serious or Rare Side Effects: - Respiratory depression: slowed breathing, potentially life‑threatening. - Severe hypotension: marked drop in blood pressure. - Hepatic injury: abnormal liver function tests. - QT interval prolongation: cardiac rhythm disturbance. - Anaphylaxis: severe allergic reaction with rash, swelling, or airway compromise. - Overdose: signs include extreme sedation, pinpoint pupils, and respiratory failure.

What precautions apply to Buprenorphine, Naloxone?

Libroxar should be prescribed after a thorough clinical assessment and patients should be monitored for safety. - Assess patient history: review prior opioid use, liver function, and psychiatric conditions. - Monitor respiratory status: watch for signs of depression, especially during initiation. - Avoid use in acute severe asthma: risk of bronchospasm. - Use caution with CNS depressants: combine only under close supervision. - Educate on sublingual administration: ensure tablet is placed under the tongue until fully dissolved. - Store at ambient temperature: keep in the original pack, protect from moisture.

What does Buprenorphine, Naloxone interact with?

Libroxar can interact with several drug classes; some combinations should be avoided while others require close monitoring.

Major Interactions (Avoid): - Opioid analgesics: additive respiratory depression risk. - Benzodiazepines: heightened sedation and respiratory compromise. - Alcohol: increased central nervous system depression. - MAO inhibitors: potential for severe hypertension or serotonin syndrome.

Moderate Interactions (Monitor Closely): - CYP3A4 inhibitors (e.g., ketoconazole): may raise buprenorphine levels. - CYP3A4 inducers (e.g., rifampicin): may reduce efficacy. - Other CNS depressants (e.g., antihistamines): monitor for enhanced sedation.

Frequently asked questions

What is Libroxar used for?+
Libroxar is indicated for the treatment of opioid dependence and opioid use disorder. It helps reduce withdrawal symptoms, cravings, and supports long‑term abstinence by providing a controlled opioid effect while blocking the actions of full opioid agonists.
How does buprenorphine/naloxone work?+
Buprenorphine acts as a partial agonist at the μ‑opioid receptor, delivering modest analgesia and mitigating withdrawal, while antagonising κ‑opioid receptors. Naloxone is poorly absorbed sublingually but becomes active if injected, blocking opioid receptors and discouraging misuse.
What is the usual dose of Libroxar?+
The appropriate dose of Libroxar is determined by the prescribing clinician based on the individual’s clinical condition, prior opioid exposure, and response to therapy. Dosage adjustments are made according to treatment guidelines and patient monitoring.
Is Libroxar safe to use during pregnancy or breastfeeding?+
Safety data for Libroxar in pregnancy and lactation are limited. Clinicians should weigh potential benefits against risks and consider alternative therapies. If used, close monitoring of the mother and infant is recommended.
How do I order Libroxar from GNH USA?+
To order Libroxar, submit an enquiry on the product page at gnh-usa.com with the required quantity. GNH USA 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.
How does Libroxar compare with other opioid dependence medications?+
Libroxar combines buprenorphine and naloxone, offering partial agonist activity with an abuse‑deterrent component. Compared with buprenorphine‑only formulations, the naloxone addition reduces the potential for intravenous misuse, while providing similar efficacy in withdrawal management.
What are the storage and handling requirements for Libroxar?+
Libroxar should be stored at ambient temperature, below 25 °C, in its original packaging. Keep the product away from moisture and direct sunlight to maintain stability.
How is Libroxar administered?+
Libroxar is administered sublingually. The tablet or film is placed under the tongue and allowed to dissolve completely without chewing or swallowing until the full dose is absorbed.
What are the most serious risks associated with Libroxar?+
Serious risks include respiratory depression, severe hypotension, hepatic injury, QT‑interval prolongation, and rare allergic reactions such as anaphylaxis. Patients should be monitored closely, especially during treatment initiation and dose changes.
Who should not use Libroxar?+
Libroxar is contraindicated in individuals with known hypersensitivity to buprenorphine, naloxone, or any excipients, and in patients with severe respiratory compromise, acute severe asthma, or uncontrolled severe hepatic impairment.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Buprenorphine, Naloxone
Route
Sublingual Use
Manufacturer
Heaton K.S.
Origin
EU

Related products