Product image of Nalidin (Naloxone Hydrochloride, Tilidine Hydrochloride) supplied by GNH India

Nalidin

Active Ingredient:
Naloxone Hydrochloride, Tilidine Hydrochloride
Origin:
EU

Nalidin (Naloxone Hydrochloride, Tilidine Hydrochloride)

Naloxone Hydrochloride, Tilidine Hydrochloride, the active ingredients in Nalidin, are a combination opioid antagonist and pro‑drug analgesic presented as an oral formulation for systemic use. It is employed to reverse opioid overdose effects and to provide analgesia for moderate pain.

GNH India supplies Nalidin 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. Customers benefit from consistent product availability and regulatory compliance support.

Manufacturer / TM Owner

Tad Pharma Gmbh

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Indications & Clinical Uses

Nalidin combines naloxone and tilidine, acting on opioid pathways to address both overdose and pain management.

  • Opioid overdose: rapidly reverses respiratory depression, sedation and other life‑threatening effects of opioid toxicity.
  • Moderate to severe pain: provides analgesia after conversion of tilidine to nortilidine, useful in acute and chronic pain settings.
  • Post‑operative pain: manages postoperative discomfort when opioid analgesia is required but rapid reversal may be needed.

How It Works

  • Naloxone hydrochloride competitively blocks μ‑opioid receptors, displacing opioid agonists and reversing their central effects. Tilidine hydrochloride is a pro‑drug that is metabolised in the liver to nortilidine, a μ‑opioid receptor agonist, producing analgesia. The combined formulation therefore offers immediate opioid antagonism together with a metabolically activated analgesic component. The antagonistic action of naloxone occurs within minutes, while tilidine’s analgesic effect develops as nortilidine reaches peak plasma concentrations within 30‑60 minutes.

Side Effects

Nalidin may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Nausea: mild to moderate feeling of sickness.
  • Dizziness: transient light‑headedness or vertigo.
  • Sweating: increased perspiration, especially during reversal of opioid effects.
  • Headache: mild to moderate head pain.

Serious or Rare Side Effects

  • Seizures: convulsive episodes, particularly in patients with predisposition.
  • Severe hypotension or hypertension: abrupt changes in blood pressure requiring medical attention.
  • Anaphylactic reaction: life‑threatening allergic response with rash, swelling, and respiratory compromise.

Precautions & Warnings

When prescribing Nalidin, consider the following precautions to ensure safe use.

  • Assess opioid dependence: evaluate risk of precipitated withdrawal before administration.
  • Monitor cardiovascular status: watch for hypertension, tachycardia or hypotension during reversal.
  • Avoid use in known hypersensitivity: contraindicated in patients allergic to naloxone or tilidine.
  • Use with caution in hepatic impairment: metabolism of tilidine may be altered, requiring close observation.
  • Pregnancy and lactation: consult specialist before use as safety data are limited.
  • Store at ambient temperature below 25°C: keep in the original packaging, protect from moisture.

Avoid Interactions

Nalidin can interact with other medicines; key interactions are categorized by clinical significance.

Major Interactions (Avoid)

  • Other opioid antagonists: additive antagonism may eliminate needed analgesia.
  • Central nervous system depressants (e.g., benzodiazepines, alcohol): risk of enhanced respiratory depression when opioid effect is abruptly reversed.

Moderate Interactions (Monitor Closely)

  • Opioid agonists: may reduce analgesic efficacy; dose adjustments may be required.
  • MAO inhibitors: can increase risk of hypertensive episodes with tilidine.
  • Serotonergic agents: potential for serotonin syndrome when combined with tilidine.

Frequently Asked Questions

Nalidin is a prescription oral medication that combines naloxone hydrochloride and tilidine hydrochloride. It is used to rapidly reverse the effects of opioid overdose and to provide analgesia for moderate to severe pain, including postoperative pain, when a controlled opioid response is required.

Naloxone hydrochloride is a competitive antagonist at μ‑opioid receptors. By binding to these receptors without activating them, it displaces opioid agonists such as morphine or heroin, quickly reversing respiratory depression, sedation and other opioid‑related effects.

The appropriate dose of Nalidin is determined by the prescribing healthcare professional based on the patient’s clinical condition, severity of opioid toxicity or pain level, and other individual factors. Dosage instructions are provided on the prescription label and should be followed exactly as directed.

Safety data for Nalidin in pregnancy and lactation are limited. Because naloxone can cross the placenta and tilidine is metabolised to an active opioid, the product should only be used if the potential benefit justifies any possible risk. Consultation with a specialist obstetrician or neonatologist is recommended.

To request Nalidin, 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 the necessary import documentation.

Unlike single‑component products, Nalidin offers both an opioid antagonist (naloxone) and a pro‑drug analgesic (tilidine) in one tablet. This dual action allows immediate reversal of opioid toxicity while still providing pain relief, which can be advantageous over using naloxone alone when analgesia is also needed.

Nalidin should be stored at ambient temperature below 25 °C, protected from moisture and direct sunlight. Keep the tablets in the original container with the lid tightly closed. Do not store in a refrigerator or freezer, and keep out of reach of children.

Nalidin is taken orally, usually as a tablet or capsule, with or without water. The exact administration schedule—whether a single dose for overdose reversal or repeated dosing for pain control—must be prescribed by a qualified healthcare professional.

The most serious risks include precipitated opioid withdrawal, severe cardiovascular changes such as abrupt hypertension or hypotension, seizures, and rare anaphylactic reactions. Patients should be monitored closely after administration, especially if they have a history of cardiovascular disease or seizure disorders.

Nalidin is contraindicated in individuals with known hypersensitivity to naloxone, tilidine, or any excipients in the formulation. It should also be avoided in patients with severe hepatic impairment without specialist supervision, and in those where rapid opioid reversal could be harmful, such as patients dependent on opioid analgesia for chronic pain without alternative pain management.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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