Reported Dec 18, 2019 · Terminated

Ranitidine Tablets, USP 150 mg, OTC, a.) 30 count bottle (NDC 68788-7078-03), b.) 60 count bottle (NDC 68788-7078-06),…

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?

    • Ranitidine Tablets
    • USP 150 mg
    • OTC
    • a.) 30 count bottle (NDC 68788-7078-03)
    • b.) 60 count bottle (NDC 68788-7078-06)
  • MfgAmneal Pharmaceuticals
Lot codes and dates
    • Lot #: I2519H
    • Exp. 12/20
    • I2719O
    • Exp. 12/20
    • J1419O
    • Exp. 12/20
    • J2819L
    • Exp. 12/20
Amount recalled
316 bottles

Where it was sold

Why it was recalled

CGMP Deviations: Presence of NDMA impurity detected in product.

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 May 9, 2023 · Data as of Sep 19, 6:34 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.