# FDA recall D-1144-2015

> **Dr. Reddy's Laboratories, Inc.** · Class III · drug recall initiated 2015-05-06.

## Product

Amlodipine besylate and Atorvastatin calcium tablets, 10mg/10mg, packaged in a)30-count bottle (NDC 43598-321-30), b) 90-count bottle (NDC 43598-321-90), Rx Only, Manufactured by Dr. Reddy's Laboratories Limited Bachupally, 500 090 India

## Reason for recall

Subpotent drug

## Distribution

Nationwide

## Key facts

- **Recall number:** D-1144-2015
- **Recalling firm:** Dr. Reddy's Laboratories, Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-05-06
- **Report date:** 2015-06-24
- **Termination date:** 2016-03-31

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Princeton, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1144-2015

## Citation

> AI Analytics. FDA recall D-1144-2015. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-1144-2015. Source: US FDA. Licensed CC0.

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