RecallRadar

FDA Drug recall D-1153-2014

Alprazolam 1 mg Tablets, USP, 500 count Bottle, Rx Only , C IV, Manufactured by: Actavis Elizabeth LLC 200 Elmora Avenue Elizabeth, NJ 0720…

On 2014-03-19 the FDA classified a Class II recall of Alprazolam 1 mg Tablets, USP, 500 count Bottle, Rx Only , C IV, Manufactured by: Actavis Elizabeth LLC 200 Elmora Avenue Elizabeth, NJ 0720… by Actavis Elizabeth, citing failed Tablet/Capsule Specifications: Complaints were received for significant tablet erosion for Alprazolam 1 mg.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1153-2014
ClassificationClass II
Statusterminated
Initiated2014-02-10
Published2014-03-19
Last updated2026-09-13 11:51 UTC
CompanyActavis Elizabeth
DistributionUS

Product

Alprazolam 1 mg Tablets, USP, 500 count Bottle, Rx Only , C IV, Manufactured by: Actavis Elizabeth LLC 200 Elmora Avenue Elizabeth, NJ 07207 USA, NDC 0228-2031-50

Reason

Failed Tablet/Capsule Specifications: Complaints were received for significant tablet erosion for Alprazolam 1 mg.

Identifiers

ndc0228-2027-10
ndc0228-2027-50
ndc0228-2027-96
ndc0228-2029-10
ndc0228-2029-50
ndc0228-2029-96
ndc0228-2031-10
ndc0228-2031-50
ndc0228-2031-96
ndc0228-2039-10
code_infoLot # 1826E131, Exp 04/2015

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1153-2014%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.