FDAFDA · Food and drugs·Recall number 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
Published August 30, 2017 · Recall initiated: April 20, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Labeling: Labeled Error on Declared Strength; report of a 1000 ct bottle labeled as Phenobarbital 15 mg tablets actually contained 30 mg tablets
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- C. O. Truxton
- Distributor
- Nationwide
- Lot
- Lot # 70952A; Exp. 11/17
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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