# FDA recall D-0110-2018

> **Osmotica Pharmaceutical Corp** · Class III · drug recall initiated 2017-12-18.

## Product

Methylphenidate Hydrochloride Extended-release Tablets, USP 27 mg, 100-count bottles,  Rx Only, Trigen Laboratories, LLC. Bridgewater, NJ 08807, NDC 13811-707-10

## Reason for recall

Subpotent Drug

## Distribution

Nationwide

## Key facts

- **Recall number:** D-0110-2018
- **Recalling firm:** Osmotica Pharmaceutical Corp
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-12-18
- **Report date:** 2017-12-27
- **Termination date:** 2019-05-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Marietta, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0110-2018

## Citation

> AI Analytics. FDA recall D-0110-2018. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/D-0110-2018. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
