# FDA recall D-0388-2022

> **Dr. Reddy's Laboratories, Inc.** · Class III · drug recall initiated 2022-01-10.

## Product

Mucus Relief D, Guaifenesin Pseudoephedrine HCl ER Tablets, 600 mg/60mg, packaged in 36-count blister pack packed into cartons, Distributed by: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, Made in India, NDC 0363-164-3

## Reason for recall

Subpotent drug

## Distribution

USA Nationwide

## Key facts

- **Recall number:** D-0388-2022
- **Recalling firm:** Dr. Reddy's Laboratories, Inc.
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2022-01-10
- **Report date:** 2022-01-26
- **Termination date:** 2024-03-29

- **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-0388-2022

## Citation

> AI Analytics. FDA recall D-0388-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/D-0388-2022. Source: US FDA. Licensed CC0.

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