# FDA recall D-1516-201

> **Lupin Limited** · Class III · drug recall initiated 2016-03-24.

## 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

- **Recall number:** D-1516-201
- **Recalling firm:** Lupin Limited
- **Classification:** Class III
- **Product type:** drug
- **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

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

## Citation

> AI Analytics. FDA recall D-1516-201. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-1516-201. Source: US FDA. Licensed CC0.

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