C. O. Truxton recalls Phenobarbital Tablets USP, 30 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp.
Labeling: Label Mixup; potentially mislabeled
Recall notice
Labeling: Label Mixup; potentially mislabeled
Contact the company & request your remedy
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Source Page by GovInfoNow · govinfonow.com/recall/41642-c-o-truxton-recalls-phenobarbital-tablets-usp-30-mg-1000 · Recall date April 20, 2017 · FDA enforcement record: FDA #D-1112-2017
Cite this page
“C. O. Truxton recalls Phenobarbital Tablets USP, 30 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp..” GovInfoNow, recall dated April 20, 2017. https://govinfonow.com/recall/41642-c-o-truxton-recalls-phenobarbital-tablets-usp-30-mg-1000. Based on FDA recall #D-1112-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1112-2017%22&limit=1).
How to tell if you have this one
- Brand
C. O. Truxton- Category
Drug
All 6 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Status
Terminated- Distribution
Nationwide
| Recall number | Product, codes & lots | Class |
|---|---|---|
| D-1111-2017 | Phenobarbital Tablets USP, 15 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6160-10; Lot # 70952A; Exp. 11/17 | Class I |
| D-1112-2017 | Phenobarbital Tablets USP, 30 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6145-10; Lot # 70926A; Exp. 11/17 Lot # 70981A; Exp. 01/18 Lot # H15A59; Exp. 08/18 | Class I |
| D-1113-2017 | Phenobarbital Tablets USP, 60 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6151-10; Lot # 71416A; Exp. 05/20 Lot # 70881A; Exp. 07/17 Lot # H15A68; Exp. 01/18 Lot # 70980A; Exp. 02/18 | Class II |
| D-1114-2017 | 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; a) Lot # 70989A; Exp. 02/18, Lot # 70973A; Exp. 01/18 b) Lot # 70973A; Exp. 01/18, Lot # H15A76; Exp. 02/18, Lot # 71346A; Exp. 12/19, Lot # 70989A; Exp. 02/18 | Class II |
| D-1115-2017 | Amitriptyline HCL Tablets, USP 50 mg, 100 count bottles, Rx Only, Manufactured for: Qualitest Pharmaceuticals Huntsville, AL 35811, Distributed by: Truxton, Inc. Bellmawr, NJ 08031, NDC: 0463-6352-10; Lot # C0260416A; Exp. 03/18 | Class II |
| D-1116-2017 | Phenobarbital Tablets USP, 15 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6160-10; Lot # 71162A; Exp. 10/18 Lot # 70915A; Exp. 08/17 Lot # H15A55; Exp. 11/17 | Class II |
Contact C. O. Truxton
We’ve drafted a message you can send C. O. Truxton to request your refund or repair — edit it as you like.
Subject: Recall D-1112-2017 — C. O. Truxton C. O. Truxton recalls Phenobarbital Tablets USP, 30 mg, 1000 count bottles, Rx Only, Hello, I own a C. O. Truxton recalls Phenobarbital Tablets USP, 30 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. that is covered by recall D-1112-2017 from C. O. Truxton. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1112-2017 (April 20, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1112-2017 to see it in context.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.