Lupin Limited recalls Escitalopram Tablets USP 20 mg, 100-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Baltimore, MD, 2120
Recalled September 28, 2016 · FDA recall D-1516-201 · Lupin
Hazard
Labeling: Incorrect or Missing Lot and/or Expiration Date · FDA Class III
Units
3,192 bottles (319,200 tablets)
Sold at
Nationwide
Description
Labeling: Incorrect or Missing Lot and/or Expiration Date
Product
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
Manufacturer(s)
Lupin Limited
Made in
India
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →