PlainRecalls
FDA Drug Moderate Class II Terminated

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

Reported: August 30, 2017 Initiated: April 20, 2017 #D-1116-2017

Product Description

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

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, 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. 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-1116-2017.