RecallRadar

FDA Drug recall D-018-2014

Alprazolam Orally Disintegrating Tablets, USP 2 mg, 100 count bottles, Rx Only, MFG. BY ACTAVIS ELIZABETH LLC., Elizabeth, NJ, NDC 0228-402…

On 2013-12-04 the FDA classified a Class II recall of Alprazolam Orally Disintegrating Tablets, USP 2 mg, 100 count bottles, Rx Only, MFG. BY ACTAVIS ELIZABETH LLC., Elizabeth, NJ, NDC 0228-402… by Actavis Elizabeth, citing failed Tablet/Capsule Specifications; partial tablet erosion resulting in tablet weights below specification in some tablets.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-018-2014
ClassificationClass II
Statusterminated
Initiated2013-10-09
Published2013-12-04
Last updated2026-09-13 11:51 UTC
CompanyActavis Elizabeth
DistributionUS

Product

Alprazolam Orally Disintegrating Tablets, USP 2 mg, 100 count bottles, Rx Only, MFG. BY ACTAVIS ELIZABETH LLC., Elizabeth, NJ, NDC 0228-4025-11

Reason

Failed Tablet/Capsule Specifications; partial tablet erosion resulting in tablet weights below specification in some tablets

Identifiers

ndc0228-4019-11
ndc0228-4022-11
ndc0228-4024-11
ndc0228-4025-11
code_infoLot # 59380831, Exp. May 2014

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-018-2014%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.