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.
Reported: December 15, 2021 Initiated: November 19, 2021 #D-0276-2022
Product Description
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.
Reason for Recall
Product Mix-up
Details
- Recalling Firm
- Ascent Pharmaceuticals, Inc.
- Units Affected
- 9744 bottles
- Distribution
- USA Nationwide
- Location
- Central Islip, NY
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Ascent Pharmaceuticals, Inc.. Units affected: 9744 bottles.
Why was this product recalled? ▼
Product Mix-up
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on December 15, 2021. Severity: Moderate. Recall number: D-0276-2022.
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