Reported Jun 5, 2013 · Terminated

Lisinopril Tablets, USP, 30 mg, Rx only, 100 tablets, NDC 65862-041-01 Manufactured for: Aurobindo Pharma USA Inc. 2400…

Aurobindo Pharma USA Inc.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Aurobindo Pharma USA Inc · 666 Plainsboro Rd. Suite 210 · Plainsboro, NJ · 08536-3004

Is this the product you have?

  • Lisinopril Tablets, USP, 30 mg, Rx only, 100 tablets
  • NDC 65862-041-01 Manufactured forAurobindo Pharma USA Inc. 2400 Route 130 North, Dayton
  • NJ 08810 Manufactured byAurobindo Pharma Limited Hyderabad- 500 072 India
Lot codes and dates
  • Lot KP3012001-A Exp.12/13 Lot KP3012002-A Exp.12/13
Amount recalled
1776 bottles

Where it was sold

  • Nationwide

Why it was recalled

Labeling: Label Error on Declared Strength: Incorrect strength on side display panel of label

This product is unlikely to cause harm, but it breaks a safety or labelling rule.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Jan 23, 2014 · Data as of Sep 19, 7:17 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.