# FDA recall D-0303-2021

> **Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals** · Class I · drug recall initiated 2021-01-27.

## Product

Spironolactone Tablets, USP, 25 mg, packaged in: a) 30-count bottles (NDC 63629-1064-01), b) 60-count bottles (NDC 63629-1064-02), c) 90-count bottles (NDC 63629-1064-03), Rx only, Manufactured by: Frontida BioPharm, Inc., Philadelphia, PA 19124 USA, Repackaged by: Bryant Ranch Prepack, Inc., Burbank, CA 91504 USA

## Reason for recall

Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 25 mg may contain spironolactone 50 mg tablets.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0303-2021
- **Recalling firm:** Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
- **Classification:** Class I
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2021-01-27
- **Report date:** 2021-03-24

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0303-2021

## Citation

> AI Analytics. FDA recall D-0303-2021. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/D-0303-2021. Source: US FDA. Licensed CC0.

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