Nalmefene Hydrochloride — Active Pharmaceutical Ingredient

Nalmefene Hydrochloride is an active pharmaceutical ingredient found in 4 FDA-approved drug products. Forms: SOLUTION, SPRAY. Routes: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS, INTRAMUSCULAR, SUBCUTANEOUS, NASAL.

This content is for informational purposes only. Always consult a healthcare professional.

Nalmefene Hydrochloride (4 brand names, 2 dosage forms, 3 routes)

Available dosage forms: SOLUTION, SPRAY.

Routes of administration: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS, INTRAMUSCULAR, SUBCUTANEOUS, NASAL.

Brand Names

  • NALMEFENE HYDROCHLORIDE
  • OPVEE
  • REVEX
  • ZURNAI (AUTOINJECTOR)

Indications and Usage

ZURNAI is indicated for the emergency treatment of known or suspected opioid overdose induced by natural or synthetic opioids in adults and pediatric patients aged 12 years and older, as manifested by respiratory and/or central nervous system depression. ZURNAI is intended for immediate administration as emergency therapy in settings where opioids may be present. ZURNAI is not a substitute for emergency medical care.

Contraindications

ZURNAI is contraindicated in patients known to be hypersensitive to nalmefene hydrochloride or to any other ingredients in the product.

Adverse Reactions

The following serious adverse reactions are described elsewhere in the labeling: Recurrent Respiratory and Central Nervous System Depression [see Warnings and Precautions (5.1)] Precipitation of Severe Opioid Withdrawal [see Warnings and Precautions (5.3)]

Mechanism of Action

ZURNAI is an antagonist at opioid receptors.

⚠ Caution
Medical Disclaimer: This information is for educational purposes only. Always consult a healthcare professional before taking any medication.