FDAFDA · Food and drugs·Recall number D-0097-2021
Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325mg 100-count bottles, Rx Only, Manufactured for : Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, Manufactured by: Ascent Pharmaceuticals, Inc. Central Islip, NY 11722, NDC 31722-943-01
Published November 25, 2020 · Recall initiated: October 26, 2020
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of Foreign Tablet/Capsule: One bottle of Hydrocodone Bitartrate and Acetaminophen Tablets USP 10mg/325 mg contains one Losartan Potassium Tablets, USP 100 mg.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Ascent Pharmaceuticals, Inc.
- Distributor
- Nationwide within the United States
- Lot
- Lot #: 20070518, Exp. Date June 2022
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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