C. O. Truxton recalls Phenobarbital Tablets USP, 100 mg, a) 100 count bottles (NDC 0463-6152-01), b) 1000 count bottles (NDC 0163-6152-10), Rx
Recalled August 30, 2017 · FDA recall D-1114-2017 · C. O. Truxton
Hazard
Labeling: Label Mixup; potentially mislabeled · FDA Class II
Units
unknown
Sold at
Nationwide
Description
Labeling: Label Mixup; potentially mislabeled
Product
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
Manufacturer(s)
C. O. Truxton
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →