Fenofibrate Capsules (Micronized) 134 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544, NDC 0115-0522-02
Reported: April 20, 2016 Initiated: March 17, 2016 #D-0820-2016
Product Description
Fenofibrate Capsules (Micronized) 134 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544, NDC 0115-0522-02
Reason for Recall
Labeling: Incorrect or Missing Lot and/or Exp. Date
Details
- Recalling Firm
- Impax Laboratories, Inc.
- Units Affected
- 28,001 HDPE bottles (14,000,500 capsules)
- Distribution
- Nationwide
- Location
- Hayward, CA
Frequently Asked Questions
What product was recalled? ▼
Fenofibrate Capsules (Micronized) 134 mg, 500-count bottle, Rx Only, Distributed by Impax Generics, Hayward, CA 94544, NDC 0115-0522-02. Recalled by Impax Laboratories, Inc.. Units affected: 28,001 HDPE bottles (14,000,500 capsules).
Why was this product recalled? ▼
Labeling: Incorrect or Missing Lot and/or Exp. Date
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 20, 2016. Severity: Low. Recall number: D-0820-2016.
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