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Alprazolam tablets, USP, CIV, 0.25 mg, Rx Only, a) 500 count bottle, b) 1000 count bottle, Distri...

FDA Recall #D-0326-2015 — Class II — December 17, 2014

Recall #D-0326-2015 Date: December 17, 2014 Classification: Class II Status: Terminated

Product Description

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 for Recall

Subpotent Drug

Recalling Firm

Neolpharma, Inc. — Caguas, PR

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Drugs

Product Quantity

12,310 bottles

Distribution

Nationwide

Code Information

Lot #: a) C100429, Exp 03/15, b) C120293, Exp 01/17

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medication immediately and contact your pharmacist or doctor. Do not flush medications down the drain. Return the product to the place of purchase for a refund or replacement.

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