Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325mg 100-count bottles, Rx Only, Manufactured for : Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, Manufactured by: Ascent Pharmaceuticals, Inc. Central Islip, NY 11722, NDC 31722-943-01
Reported: November 25, 2020 Initiated: October 26, 2020 #D-0097-2021
Product Description
Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325mg 100-count bottles, Rx Only, Manufactured for : Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, Manufactured by: Ascent Pharmaceuticals, Inc. Central Islip, NY 11722, NDC 31722-943-01
Reason for Recall
Presence of Foreign Tablet/Capsule: One bottle of Hydrocodone Bitartrate and Acetaminophen Tablets USP 10mg/325 mg contains one Losartan Potassium Tablets, USP 100 mg.
Details
- Recalling Firm
- Ascent Pharmaceuticals, Inc.
- Units Affected
- 9768 Bottles
- Distribution
- Nationwide within the United States
- Location
- Central Islip, NY
Frequently Asked Questions
What product was recalled? ▼
Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325mg 100-count bottles, Rx Only, Manufactured for : Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, Manufactured by: Ascent Pharmaceuticals, Inc. Central Islip, NY 11722, NDC 31722-943-01. Recalled by Ascent Pharmaceuticals, Inc.. Units affected: 9768 Bottles.
Why was this product recalled? ▼
Presence of Foreign Tablet/Capsule: One bottle of Hydrocodone Bitartrate and Acetaminophen Tablets USP 10mg/325 mg contains one Losartan Potassium Tablets, USP 100 mg.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 25, 2020. Severity: Moderate. Recall number: D-0097-2021.
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