RecallRadar

FDA Drug recall D-0326-2015

Alprazolam tablets, USP, CIV, 0.25 mg, Rx Only, a) 500 count bottle, b) 1000 count bottle, Distributed by: Greenstone LLC, Peapack, NJ, 079…

On 2014-12-31 the FDA classified a Class II recall of Alprazolam tablets, USP, CIV, 0.25 mg, Rx Only, a) 500 count bottle, b) 1000 count bottle, Distributed by: Greenstone LLC, Peapack, NJ, 079… by Neolpharma, citing subpotent Drug.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0326-2015
ClassificationClass II
Statusterminated
Initiated2014-12-17
Published2014-12-31
Last updated2026-09-13 11:51 UTC
CompanyNeolpharma
DistributionUS

Product

Alprazolam tablets, USP, CIV, 0.25 mg, Rx Only, a) 500 count bottle, b) 1000 count bottle, Distributed by: Greenstone LLC, Peapack, NJ, 07977, a) NDC 59762-3719-3, b) NDC 59762-3719-4.

Reason

Subpotent Drug

Identifiers

ndc59762-3719-1
ndc59762-3719-3
ndc59762-3719-4
ndc59762-3720-1
ndc59762-3720-3
ndc59762-3720-4
ndc59762-3721-1
ndc59762-3721-3
ndc59762-3721-4
ndc59762-3722-1
ndc59762-3722-3
code_infoLot #: a) C100429, Exp 03/15, b) C120293, Exp 01/17

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-0326-2015%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.