Reported Nov 29, 2017 · Terminated

Pravastatin Sodium USP, tablets, 40 mg, 90-count bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc.,…

Lupin Limited

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: Lupin Limited · 15 - B I Phase 1a · Vasco Da Gama, N/A · N/A

Is this the product you have?

  • Pravastatin Sodium USP, tablets, 40 mg, 90-count bottle, Rx only
  • Manufactured forLupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, NDC 68180-487-09
Lot codes and dates
    • Lot # G702459
    • Exp 2/20
Amount recalled
N/A

Where it was sold

Why it was recalled

Presence of foreign tablets/capsules: This product lot is being recalled due to a pharmacy complaint where one Duloxetine Delayed Release Capsule, 30mg was found in a Pravastatin Sodium Tablets USP, 40mg bottle.

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 15, 2019 · Data as of Sep 19, 8:07 PM UTC

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