FDAFDA · Food and drugs·Recall number D-0276-2022
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.
Published December 15, 2021 · Recall initiated: November 19, 2021
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
Product Mix-up
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- HYDROCODONE BITARTRATE AND ACETAMINOPHEN
- Manufacturer
- Ascent Pharmaceuticals, Inc.
- Distributor
- USA Nationwide
- UPC
- 0331722997010
- Lot
- Lot #: 21070817, Exp 6/2023
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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