FDAFDA · Food and drugs·Recall number D-1516-201
Escitalopram Tablets USP 20 mg, 100-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Baltimore, MD, 21202, Manufactured by: Lupin Limited, Goa 403 722, India, NDC 68180-136-01
Published September 28, 2016 · Recall initiated: March 24, 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 Expiration Date
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Brand
- ESCITALOPRAM
- Manufacturer
- Lupin Limited
- Distributor
- Nationwide
- UPC
- 0368180135012
- Lot
- Lot # G510086; Exp. 11/17
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- India
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