Orexigen Therapeutics, Inc. recalls Contrave (naltrexone HCl and bupropion HCl). Extended-Release Tablets, 8mg/90 mg, 120-count bottles, Rx only, Distribut…
- Recall date
- October 5, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0219-2019
- FDA classification
- Class III
- Brand / firm
- Orexigen Therapeutics, Inc.
- Sold / distributed
- Within the United States
Why it was recalled
Container packaging defect.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Contrave (naltrexone HCl and bupropion HCl). Extended-Release Tablets, 8mg/90 mg, 120-count bottles, Rx only, Distributed by Orexigen therapeutics, Inc., La Jolla, CA 92037, NDC 51267-890-99
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