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Class II: temporary or reversible health riskTerminated

Dr. Reddy's Laboratories Divalproex Sodium Extended-Release Tablets Recall

Divalproex Sodium Extended-Release Tablets, USP, 500 mg, 100 count bottles, Rx Only, Mfd

Dr. Reddy's Laboratories, Inc. · Princeton, NJ

Risk level
Class II
Reported by FDA
Jun 24, 2015
Recall ID
D-1136-2015
Check your lot numberHow we source this data

Summary

Dr. Reddy's Laboratories recalled Divalproex Sodium Extended-Release Tablets starting May 22, 2015. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-1136-2015 on Jun 24, 2015. Reason: Failed Dissolution Specifications; exceeded specification at the 9 hour time point. Status: Terminated.

Why it was recalled

Failed Dissolution Specifications; exceeded specification at the 9 hour time point

Product description

Divalproex Sodium Extended-Release Tablets, USP, 500 mg, 100 count bottles, Rx Only, Mfd. By. Dr. Reddy's Laboratories Limited Bachupally 500 090 India --- NDC 55111-534-01

Lot numbers, UPCs & expiration codes

Lot #C308195, exp 10/2015

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-1136-2015
Classification
Class II
Status
Terminated
Recall initiated
May 22, 2015
FDA report date
Jun 24, 2015
Quantity
5,160 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Dr. Reddy's Laboratories, Inc.

Original FDA data

Every field from FDA enforcement report D-1136-2015, exactly as published.

Show all FDA fields
City
Princeton
State
NJ
Status
Terminated
Country
United States
Event ID
71374
Address
107 College Rd E
Code information
Lot #C308195, exp 10/2015
Postal code
08540-6623
Report date
Jun 24, 2015
Product type
Drugs
Recall number
D-1136-2015
Classification
Class II
Recalling firm
Dr. Reddy's Laboratories, Inc.
Product quantity
5,160 bottles
Termination date
Apr 24, 2017
Reason for recall
Failed Dissolution Specifications; exceeded specification at the 9 hour time point
Voluntary / mandated
Voluntary: Firm initiated
Product description
Divalproex Sodium Extended-Release Tablets, USP, 500 mg, 100 count bottles, Rx Only, Mfd. By. Dr. Reddy's Laboratories Limited Bachupally 500 090 India --- NDC 55111-534-01
Distribution pattern
Nationwide
Recall initiation date
May 22, 2015
Initial firm notification
Letter
Center classification date
Jun 12, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1136-2015, published Jun 24, 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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