Home / Recalls / Lupin Limited / D-1516-201

D-1516-201 Class III Terminated

Recalled by Lupin Limited — Verna, Salcette, Goa

Recall Details

Product Type
Drugs
Report Date
September 28, 2016
Initiation Date
March 24, 2016
Termination Date
March 15, 2017
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
3,192 bottles (319,200 tablets)

Product Description

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

Reason for Recall

Labeling: Incorrect or Missing Lot and/or Expiration Date

Distribution Pattern

Nationwide

Code Information

Lot # G510086; Exp. 11/17

Other recalls by Lupin Limited

  • D-0092-2018 Class II — Pravastatin Sodium USP, tablets, 40 mg, 90-count bottle, Rx only, Manufactured f (November 17, 2017)
  • D-1493-2016 Class III — Amlodipine Besylate Tablets USP, 10mg, 1000-count bottles, Rx only, Manufactured (February 19, 2016)
  • D-1492-2016 Class III — Amlodipine Besylate Tablets USP, 2.5mg, 90-count bottles, Rx only, Manufactured (February 19, 2016)