Reported Mar 18, 2020 · Terminated

Ranitidine Tablets, USP, 150 mg, 100 Tablets (10 tablets x 10 blister card), Rx Only, Packaged and Distributed by:…

American Health Packaging

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: American Health Packaging · 2550 John Glenn Ave Ste A · Columbus, OH · 43217-1188

Is this the product you have?

  • Ranitidine Tablets, USP, 150 mg, 100 Tablets (10 tablets x 10 blister card), Rx Only
  • Packaged and Distributed byAmerican Health Packaging, Columbus, Ohio 43217
  • NDC carton60687-322-01
  • NDC Unit Dose Card60687-322-11
Lot codes and dates
  • Lot
  • expiry
    • Lots 179516
    • 179745
    • exp 12/31/2019
    • Lot 180712
    • exp 02/29/2020
    • Lot 180819
    • exp 04/30/2020
    • Lots 181403
    • 182544
    • 183155
    • 183236
    • exp 05/31/2020
    • Lots 185739
    • 186600
    • 186702
    • exp 12/31/2020
Amount recalled
53,619 cartons

Where it was sold

  • Nationwide

Why it was recalled

CGMP Deviations: Potential N-Nitrosodimethylamine (NDMA) amounts above levels established by the FDA.

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

Want the full recall guide?

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Where this came from

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

Read the FDA (openFDA drug enforcement) notice

Notice updated Aug 4, 2022 · Data as of Sep 19, 7:53 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.