# FDA recall D-0844-2022

> **Viatris Inc** · Class II · drug recall initiated 2022-04-28.

## Product

alprazolam XR extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by: Greenstone LLC, Peapack, NJ  07977, NDC 59762-0068-1.

## Reason for recall

Failed Dissolution Specifications: low out-of-specification dissolution test results observed.

## Distribution

Product was distributed nationwide in the USA

## Key facts

- **Recall number:** D-0844-2022
- **Recalling firm:** Viatris Inc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2022-04-28
- **Report date:** 2022-05-11
- **Termination date:** 2023-06-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Canonsburg, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0844-2022

## Citation

> AI Analytics. FDA recall D-0844-2022. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0844-2022. Source: US FDA. Licensed CC0.

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