Ascent Pharmaceuticals, Inc. recalls Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325 mg, 100-count bottle, Rx only, Manufactured for: Camber
Recalled December 15, 2021 · FDA recall D-0276-2022 · Ascent Pharmaceuticals
Hazard
Product Mix-up · FDA Class II
Units
9744 bottles
Sold at
USA Nationwide
Description
Product Mix-up
Product
Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325 mg, 100-count bottle, Rx only, Manufactured for: Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, Manufactured by: Ascent Pharmaceuticals, Inc., Central Islip, NY 11722, NDC 31722-997-01.
Manufacturer(s)
Ascent Pharmaceuticals, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →