FDAFDA · Food and drugs·Recall number D-1528-2016
PREMARIN (conjugated estrogen tablets, USP) 1.25 mg, 1000- count bottle, Rx only, Distributed by: Wyeth Pharmaceuticals Inc. A subsidiary of Pfizer Inc. Philadelphia, PA 19101, NDC 0046-1104-91
Published October 5, 2016 · Recall initiated: September 15, 2016
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: Incorrect or Missing Lot and/or Exp Date: Bottles were incorrectly labeled with an expiry date of 11/17; the correct date is 09/17.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- PREMARIN
- Manufacturer
- Pfizer Inc.
- Distributor
- Nationwide
- UPC
- 0300461100913
- Lot
- Lot # M35953S; Exp. 11/17 (labeled).
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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