FDAFDA · Food and drugs·Recall number D-0291-2015
Fluoxetine Capsules USP, 20 mg, 100 count bottle, Rx Only, 100 Capsules, Sandoz Inc Princeton, NJ 08540 NDC 0781-2822-01
Published December 17, 2014 · Recall initiated: December 5, 2014
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
Labeling: Illegible Label: Sandoz Inc. is recalling of one lot of Fluoxetine Capsules due to an illegible logo on the capsule.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Sandoz Incorporated
- Distributor
- AZ
- Lot
- Lot ET5122, Exp. 10/17
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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