FDAFDA · Food and drugs·Recall number D-0507-2017
Zenatane (isotretinoin) capsules, 20 mg, packaged in 30-count cartons (3 x 10 blister cards), Rx Only, Manufactured By:Cipla Limited Kurkumbh Village Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 55111-136-81
Published March 8, 2017 · Recall initiated: February 15, 2017
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 dissolution specifications - low dissolution results at S3 stage.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- ZENATANE
- Manufacturer
- Dr. Reddy's Laboratories, Inc.
- Distributor
- U.S. Nationwide
- Lot
- Lot # KB50877, KB50878, Exp 11/17; KB50878, 01KB60251, Exp 3/18
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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