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Class III: unlikely to cause harmTerminated

Par Pharmaceutical Meclizine Hydrochloride Tablets Recall

Meclizine Hydrochloride Tablets USP, 25 mg Tablets, Packaged in a) 100 Ct Bottles (NDC:…

Par Pharmaceutical Inc. · Spring Valley, NY

Risk level
Class III
Reported by FDA
Nov 25, 2015
Recall ID
D-0234-2016
Check your lot numberHow we source this data

Summary

Par Pharmaceutical recalled Meclizine Hydrochloride Tablets starting Oct 26, 2015. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-0234-2016 on Nov 25, 2015. Reason: Failed Impurities/Degradation Specifications: Out of specification for impurities. Status: Terminated.

Why it was recalled

Failed Impurities/Degradation Specifications: Out of specification for impurities.

Product description

Meclizine Hydrochloride Tablets USP, 25 mg Tablets, Packaged in a) 100 Ct Bottles (NDC: 49884-035-01) and b) 1000 Ct Bottles (NDC: 49884-035-10), Rx only. Par Pharmaceutical Companies, Inc., Spring Valley, NY 10977.

Lot numbers, UPCs & expiration codes

a) Lot #: 25552101, Expiry: AUG 2016; Lot#: 25712701, Expiry: SEP 2016; Lot #: 25787902, Expiry: NOV 2016; Lot #: 26074601, Expiry: JAN 2017; Lot #: 26259801, Expiry: APR 2017; Lot #: 26220001, Expiry: MAR 2017; Lot #: 26579001, Expiry: JUN 2017; Lot #: 26731801, Expiry: NOV 2017. b) Lot #: 24502301, Expiry: OCT 2015; Lot #: 24505901, Expiry: OCT 2015; Lot #: 25787901, Expiry: NOV 2016; Lot #: 26074701, Expiry: JAN 2017; Lot #: 26259701, Expiry: MAR 2017; Lot #: 26575801, Expiry: JUN 2017; Lot #: 26579002, Expiry: JUN 2017; Lot #: 26682801, Expiry: SEP 2017; Lot #: 26682901, Expiry: SEP 2017; Lot #: 26731702, Expiry: NOV 2017; Lot #: 25960301, Expiry: NOV 2017; Lot #: 26764801, Expiry: MAR 2018.

Where it was sold

U.S. Nationwide including Puerto Rico

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-0234-2016
Classification
Class III
Status
Terminated
Recall initiated
Oct 26, 2015
FDA report date
Nov 25, 2015
Quantity
a) 387,100 Bottles; b) 63,572 Bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Par Pharmaceutical Inc.

Original FDA data

Every field from FDA enforcement report D-0234-2016, exactly as published.

Show all FDA fields
City
Spring Valley
State
NY
Status
Terminated
Country
United States
Event ID
72476
Address
1 Ram Ridge Rd
Code information
a) Lot #: 25552101, Expiry: AUG 2016; Lot#: 25712701, Expiry: SEP 2016; Lot #: 25787902, Expiry: NOV 2016; Lot #: 26074601, Expiry: JAN 2017; Lot #: 26259801, Expiry: APR 2017; Lot #: 26220001, Expiry: MAR 2017; Lot #: 26579001, Expiry: JUN 2017; Lot #: 26731801, Expiry: NOV 2017. b) Lot #: 24502301, Expiry: OCT 2015; Lot #: 24505901, Expiry: OCT 2015; Lot #: 25787901, Expiry: NOV 2016; Lot #: 26074701, Expiry: JAN 2017; Lot #: 26259701, Expiry: MAR 2017; Lot #: 26575801, Expiry: JUN 2017; Lot #: 26579002, Expiry: JUN 2017; Lot #: 26682801, Expiry: SEP 2017; Lot #: 26682901, Expiry: SEP 2017; Lot #: 26731702, Expiry: NOV 2017; Lot #: 25960301, Expiry: NOV 2017; Lot #: 26764801, Expiry: MAR 2018.
Postal code
10977-6714
Report date
Nov 25, 2015
Product type
Drugs
Recall number
D-0234-2016
Classification
Class III
Recalling firm
Par Pharmaceutical Inc.
Product quantity
a) 387,100 Bottles; b) 63,572 Bottles
Termination date
Apr 20, 2017
Reason for recall
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Meclizine Hydrochloride Tablets USP, 25 mg Tablets, Packaged in a) 100 Ct Bottles (NDC: 49884-035-01) and b) 1000 Ct Bottles (NDC: 49884-035-10), Rx only. Par Pharmaceutical Companies, Inc., Spring Valley, NY 10977.
Distribution pattern
U.S. Nationwide including Puerto Rico
Recall initiation date
Oct 26, 2015
Initial firm notification
Letter
Center classification date
Nov 13, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0234-2016, published Nov 25, 2015. 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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