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.

FDA recall notice · announced December 31, 2014 · Neolpharma

Class II FDA/FSIS Class II: use may cause temporary or medically reversible adverse health consequences.

The 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 for recall

Subpotent Drug

Notes

Distribution: Nationwide
Lot/code information: Lot #: a) C100429, Exp 03/15, b) C120293, Exp 01/17
Quantity: 12,310 bottles
Status: Terminated
Products in this recall event:
- 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. (D-0326-2015)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.