Impax Laboratories, Inc. recalls Fenofibrate Capsules (Micronized) 200 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544,…
- Recall date
- March 17, 2016
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0821-2016
- FDA classification
- Class III
- Brand / firm
- Impax Laboratories, Inc.
- Sold / distributed
- Nationwide
Why it was recalled
Labeling: Incorrect or Missing Lot and/or Exp. Date
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Fenofibrate Capsules (Micronized) 200 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544, NDC 0115-0533-02
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