Reported Oct 17, 2018 · Terminated

Pantoprazole Sodium Delayed-Release Tablets, USP, 40 mg*, 90-count bottle, Rx only, Manufactured by

Jubilant Cadista 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: Jubilant Cadista Pharmaceuticals, Inc. · 207 Kiley Dr · Salisbury, MD · 21801-2249

Is this the product you have?

Pantoprazole Sodium Delayed-Release Tablets, USP, 40 mg*, 90-count bottle, Rx only, Manufactured by

3 of 3 products

Products covered by this recall
#Product as published
1Jubilant Generics Ltd., Roorkee - 247661, India
2Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801
3NDC 59746-284-90.
Lot codes and dates
    • Lot #: PA26038A
    • Exp 04/19
    • PA26039A
    • PA26040A
    • PA26050A
    • Exp 05/19
    • PA26052A
    • Exp 06/19
    • PA26073A
    • Exp 07/19
    • PA217071A
    • PA217072A
    • PA217073B
    • PA217074B
    • Exp 06/20
    • PA217101A
    • Exp 08/20
    • and PA218023A
    • Exp 01/21
Amount recalled
158,466 bottles

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Discoloration: Presence of dark discoloration or brown spots on the edges of the tablets.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

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

Read the FDA (openFDA drug enforcement) notice

Notice updated Feb 24, 2020 · Data as of Sep 19, 6:38 PM UTC

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