Reported Mar 27, 2019 · Terminated

Losartan Potassium Tablets, USP, 50 mg, a) 30-count bottle (NDC: 68788-0048-03), b) 90-count bottle (NDC:…

Preferred Pharmaceuticals, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

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: Preferred Pharmaceuticals, Inc · 1250 N Lakeview Ave Ste O · Anaheim, CA · 92807-1801

Is this the product you have?

  • Losartan Potassium Tablets, USP, 50 mg
  • a) 30-count bottle (NDC68788-0048-03)
  • b) 90-count bottle (NDC68788-0048-09), Rx Only
  • MfgTorrent Pharma Inc. Basking Ridge, NJ
  • Relabeled byPreferred Pharmaceuticals, Inc. 1250 N. Lakeview Ave., Suite O, Anaheim, CA 92807
Lot codes and dates
  • Count, lots
  • expiry
    • a) 30-count bottle C2218C
    • exp 9/2020
    • D1318E
    • exp 10/2020
    • b) 90-count bottle C2719J
    • exp 9/2020
    • E1818B
    • exp 10/2020
Amount recalled
530

Where it was sold

Why it was recalled

CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) was identified.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

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

Read the FDA (openFDA drug enforcement) notice

Notice updated Mar 30, 2023 · Data as of Sep 19, 8:08 PM UTC

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