PlainRecalls
FDA Drug Moderate Class II Terminated

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

Reported: August 30, 2017 Initiated: April 20, 2017 #D-1114-2017

Product Description

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

Reason for Recall

Labeling: Label Mixup; potentially mislabeled

Details

Recalling Firm
C. O. Truxton
Units Affected
unknown
Distribution
Nationwide
Location
Bellmawr, NJ

Frequently Asked Questions

What product was recalled?
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. Recalled by C. O. Truxton. Units affected: unknown.
Why was this product recalled?
Labeling: Label Mixup; potentially mislabeled
Which agency issued this recall?
This recall was issued by the FDA Drug on August 30, 2017. Severity: Moderate. Recall number: D-1114-2017.