Hydrocodone Bitartrate and Acetaminophen Tablets recall
Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325 mg, 100-count bottle, Rx only, Manufactured for: Camber Pharmaceuticals, Inc.…
Why was Hydrocodone Bitartrate and Acetaminophen Tablets recalled?
Product Mix-up
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 21070817, Exp 6/2023
- Product
- Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325 mg, 100-count bottle, Rx only, Manufactured for: Camber Pharmaceuticals, Inc.…
- Recalling firm
- Ascent Pharmaceuticals, Inc.
- Quantity
- 9744 bottles
- Distribution
- USA Nationwide
- Recall date
- December 15, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)