# FDA recall D-041-2013

> **Aurobindo Pharma LTD** · Class II · drug recall initiated 2012-03-09.

## Product

Northstar Zolpidem Tartrate Tablets USP 10 mg.  Manufactured for Northstar RX, LLC Memphis, TN 38141.  Manufactured by Aurobindo Pharma Limited, Unit VII, Mahaboob Dagar, 509302, India

## Reason for recall

Adulterated Presence of Foreign Tablets: This product is being recalled becaiuse 30 valacyclovir hydrochloride tablets USP 500 mg were discovered in a bottle labeled Zolpidem Tartrate tables USP 10 mg

## Distribution

Nationwide

## Key facts

- **Recall number:** D-041-2013
- **Recalling firm:** Aurobindo Pharma LTD
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-03-09
- **Report date:** 2012-11-14
- **Termination date:** 2013-11-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mehbubnagar, N/A, India

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-041-2013

## Citation

> AI Analytics. FDA recall D-041-2013. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-041-2013. Source: US FDA. Licensed CC0.

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