FDAFDA · Food and drugs·Recall number D-009-2014
Omeprazole Delayed-Release Capsules, USP, 20 mg, Rx Only, 1000 Capsules per bottle, Distributed by: Kremers Urban Pharmaceuticals Inc. Princeton, NJ 08540, USA, NDC: 62175-118-43
Published November 27, 2013 · Recall initiated: September 16, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Tablet/Capsule Specification: some capsules over time do not meet or are suspected to not meet the specification for acid resistance.
What to do
Voluntary: Firm initiated
Recall details
- Brand
- OMEPRAZOLE
- Manufacturer
- Kremers Urban Pharmaceuticals, Inc.
- Distributor
- KY & TN
- UPC
- 0362175136329
- Lot
- Lot Number 59627; Expiration Date 02/2014
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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