US FDA working on OTC naloxone to alleviate opioid crisis

23 September 2019
fda_big

The US Food and Drug Administration has issued an update on efforts to increase the availability of all forms of naloxone products, with the aim of combating the opioid crisis.

The agency said that, while naloxone is “a critical tool for individuals, families, first responders and communities to help reduce opioid overdose deaths,” access remains limited in some parts of the country.

All three forms of naloxone - injectable, auto-injector and nasal spray - currently require a prescription, but many US States have passed laws that allow pharmacists to dispense naloxone under special rules.

This article is accessible to registered users, to continue reading please register for free.  A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.

Login to your account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed

Chairman, Sanofi Aventis UK



Today's issue

Company Spotlight





More Features in Pharmaceutical