EMBEDA- morphine sulfate and naltrexone hydrochloride capsule, extended release 
Pfizer Laboratories Div Pfizer Inc


Medication Guide

EMBEDA® (im-bed-a)
(morphine sulfate and naltrexone hydrochloride) extended-release capsules, CII


Important information about EMBEDA:

Do not take EMBEDA if you have:

Before taking EMBEDA, tell your healthcare provider if you have a history of:

  • head injury, seizures
  • problems urinating
  • liver, kidney, thyroid problems
  • pancreas or gallbladder problems
  • abuse of street or prescription drugs, alcohol addiction, or mental health problems.

Tell your healthcare provider if you are:

When taking EMBEDA:

While taking EMBEDA DO NOT:

The possible side effects of EMBEDA are:

Get emergency medical help if you have:

These are not all the possible side effects of EMBEDA. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. For more information go to dailymed.nlm.nih.gov

Manufactured for: Pfizer Inc, New York, NY 10017 by: Actavis Elizabeth LLC, 200 Elmora Avenue, Elizabeth, NJ 07207, www.embeda.com or call 1-800-438-1985

This Medication Guide has been approved by the U.S. Food and Drug Administration

Revised: April 2014; LAB-0643-1.0

Revised: 10/2014
Document Id: c1650481-a5de-4c70-ba40-d80f8f0f3384
Set id: a7658a2d-b7a9-4fb5-8d65-a20ca1b9ad1f
Version: 12
Effective Time: 20141021
Pfizer Laboratories Div Pfizer Inc