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
Reported: November 14, 2018 Initiated: October 5, 2018 #D-0219-2019
Product Description
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
Reason for Recall
Container packaging defect.
Details
- Recalling Firm
- Orexigen Therapeutics, Inc.
- Units Affected
- 18,895 bottles
- Distribution
- Within the United States
- Location
- La Jolla, CA
Frequently Asked Questions
What product 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. Recalled by Orexigen Therapeutics, Inc.. Units affected: 18,895 bottles.
Why was this product recalled? ▼
Container packaging defect.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 14, 2018. Severity: Low. Recall number: D-0219-2019.
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