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
Reported: February 7, 2018 Initiated: January 22, 2018 #D-0248-2018
Product Description
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
Reason for Recall
Labeling; Label Error Not Elsewhere Classified; label missing controlled substance CII symbol
Details
- Recalling Firm
- Ascent Pharmaceuticals, Inc.
- Units Affected
- 45,875 bottles
- Distribution
- Nationwide
- Location
- Central Islip, NY
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Ascent Pharmaceuticals, Inc.. Units affected: 45,875 bottles.
Why was this product recalled? ▼
Labeling; Label Error Not Elsewhere Classified; label missing controlled substance CII symbol
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 7, 2018. Severity: Low. Recall number: D-0248-2018.
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