Reported Feb 2, 2022 · Terminated

Metoprolol Succinate Extended-Release Tablets, USP 50 mg, 500-count bottle, Rx Only, Manufactured by: Alkem…

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?

  • Metoprolol Succinate Extended-Release Tablets, USP 50 mg, 500-count bottle, Rx Only
  • Manufactured byAlkem Laboratories Ltd., Mumbai - 400 013 INDIA. NDC 68001-501-03
Lot codes and dates
    • Lots# 21141983
    • 21141984 and 21141985
    • Exp 03/31/2023
    • Lots# 21142017
    • 21142018
    • 21142019
    • Exp 02/28/2023
Amount recalled
6,637 500-count bottles

Where it was sold

  • Nationwide

Why it was recalled

Failed Dissolution Specifications

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 9, 2023 · Data as of Sep 19, 6:35 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.