FDAFDA · Food and drugs·Recall number D-0248-2018
Oxycodone Hydrochloride Tablets, USP 15 mg, 100 count bottles, Rx only, Manufactured for Camber Pharmaceuticals, Inc., Piscataway, NJ, Manufactured by: Ascent Pharmaceuticals, Inc., Central Islip, NY --- NDC 31722-917-01
Published February 7, 2018 · Recall initiated: January 22, 2018
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
Labeling; Label Error Not Elsewhere Classified; label missing controlled substance CII symbol
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- OXYCODONE HYDROCHLORIDE
- Manufacturer
- Ascent Pharmaceuticals, Inc.
- Distributor
- Nationwide
- UPC
- 0331722917018
- Lot
- Lot Numbers: 17080591 and 17080619, exp 07/19; 17110907 and 17110908, exp 10/19; and 17120986, exp 11/19
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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