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Class II: temporary or reversible health riskTerminated

Neolpharma Alprazolam tablets Recall

Alprazolam tablets, USP, CIV, 0

Neolpharma, Inc. · Caguas, PR

Risk level
Class II
Reported by FDA
Dec 31, 2014
Recall ID
D-0326-2015
Check your lot numberHow we source this data

Summary

Neolpharma recalled Alprazolam tablets starting Dec 17, 2014. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0326-2015 on Dec 31, 2014. Reason: Subpotent Drug. Status: Terminated.

Why it was recalled

Subpotent Drug

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.

Lot numbers, UPCs & expiration codes

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

Where it was sold

Nationwide

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0326-2015
Classification
Class II
Status
Terminated
Recall initiated
Dec 17, 2014
FDA report date
Dec 31, 2014
Quantity
12,310 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Neolpharma, Inc.

Original FDA data

Every field from FDA enforcement report D-0326-2015, exactly as published.

Show all FDA fields
City
Caguas
State
PR
Status
Terminated
Country
United States
Event ID
69985
Address
99 Calle Jardines
Code information
Lot #: a) C100429, Exp 03/15, b) C120293, Exp 01/17
Postal code
00725-3382
Report date
Dec 31, 2014
Product type
Drugs
Recall number
D-0326-2015
Classification
Class II
Recalling firm
Neolpharma, Inc.
Product quantity
12,310 bottles
Termination date
Apr 26, 2017
Reason for recall
Subpotent Drug
Voluntary / mandated
Voluntary: Firm initiated
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.
Distribution pattern
Nationwide
Recall initiation date
Dec 17, 2014
Initial firm notification
Letter
Center classification date
Dec 24, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0326-2015, published Dec 31, 2014. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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