Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Phenobarbital Tablets USP Recalled by C. O. Truxton Due to Mislabeling
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact C. O. Truxton directly.
Affected Products
Phenobarbital Tablets USP, 100 mg, a) 100 count bottles (NDC 0463-6152-01), b) 1000 count bottles (NDC 0163-6152-10), Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031
Quantity: unknown
Why Was This Recalled?
Labeling: Label Mixup; potentially mislabeled
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About C. O. Truxton
C. O. Truxton has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report