Reported Jan 23, 2019 · Terminated

Olmesartan Medoxomil and Hydrochlorothiazide Tablets, 40 mg/25 mg, packaged in a) 30-count bottle (NDC 0093-7617-56),…

Teva Pharmaceuticals USA

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: Teva Pharmaceuticals USA · 1090 Horsham Rd · North Wales, PA · 19454-1505

Is this the product you have?

  • Olmesartan Medoxomil and Hydrochlorothiazide Tablets, 40 mg/25 mg, packaged in a) 30-count bottle (NDC 0093-7617-56), b) 90-count bottle (NDC 0093-7617-98), Rx only
  • Manufactured In Israel ByTeva Pharmaceutical, IND. LTD., Jerusalem, 9777402, Israel
  • Manufactured ForTeva Pharmaceutical USA, INC., North Wales, PA 19454
Lot codes and dates
    • Lot #: a) 49O005
    • 49O006
    • 49O007
    • 49O010
    • Exp 02/2019
    • b) 49O005
    • 49O009
    • 49O010
    • Exp 02/2019
Amount recalled
181,456 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 Aug 31, 2020 · Data as of Sep 19, 8:01 PM UTC

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