# FDA recall D-0703-2021

> **SUN PHARMACEUTICAL INDUSTRIES INC** · Class II · drug recall initiated 2021-07-29.

## Product

Venlafaxine Tablets, USP 50 mg*, 100 Tablets  Manufactured for Northstar Rx LLC Memphis, TN 38141 Manufactured by: ALKALOIDA Chemical Company Zrt. 4440 Tiszavasvari, Kabay Janos u.29.Hungary. Product of India NDC 16714-657-01

## Reason for recall

Presence of Forein Tablets/Capsules; Venlafaxine Tablets, USP 37.5 mg found in bottles labeled as Venlafaxine Tablets, USP, 50 mg

## Distribution

Northstar Distribution Center 4853 Crumpler Rd. Memphis, TN 38141

## Key facts

- **Recall number:** D-0703-2021
- **Recalling firm:** SUN PHARMACEUTICAL INDUSTRIES INC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2021-07-29
- **Report date:** 2021-08-18
- **Termination date:** 2023-06-08

- **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-0703-2021

## Citation

> AI Analytics. FDA recall D-0703-2021. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/D-0703-2021. Source: US FDA. Licensed CC0.

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