# FDA recall D-1051-2019

> **Preferred Pharmaceuticals, Inc** · Class II · drug recall initiated 2019-03-06.

## Product

Losartan Potassium Tablets, USP, 50 mg, a) 30-count bottle (NDC: 68788-0048-03), b) 90-count bottle (NDC: 68788-0048-09), Rx Only, Mfg: Torrent Pharma Inc. Basking Ridge, NJ. Relabeled by: Preferred Pharmaceuticals, Inc. 1250 N. Lakeview Ave., Suite O, Anaheim, CA 92807.

## Reason for recall

CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) was identified.

## Distribution

California, Georgia, Indiana

## Key facts

- **Recall number:** D-1051-2019
- **Recalling firm:** Preferred Pharmaceuticals, Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-03-06
- **Report date:** 2019-03-27
- **Termination date:** 2023-03-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Anaheim, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1051-2019

## Citation

> AI Analytics. FDA recall D-1051-2019. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/D-1051-2019. Source: US FDA. Licensed CC0.

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