Lupin Limited recalls Escitalopram Tablets USP 20 mg, 100-count bottles, Rx Only, Manufactured for: Lupin Pharmaceuticals, Baltimore, MD, 212…

Recall date

March 24, 2016

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-1516-201

FDA classification

Class III

Brand / firm

Lupin Limited

Sold / distributed

Nationwide

Why it was recalled

Labeling: Incorrect or Missing Lot and/or Expiration Date

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

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