FDA recall D-1516-201

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

Reason for recall

Labeling: Incorrect or Missing Lot and/or Expiration Date

Distribution

Nationwide

Key facts

Status

Terminated

Initiation date

2016-03-24

Report date

2016-09-28

Termination date

2017-03-15

Voluntary/Mandated

Voluntary: Firm initiated

Location

Verna, Salcette, Goa, India

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1516-201