# FDA recall D-1079-2014

> **Corepharma LLC** · Class II · drug recall initiated 2013-12-13.

## Product

Pyridostigmine Bromide Tablets USP, 60 mg, 100 count bottle, Rx only, Manufactured and Distributed by: Corepharma, LLC Middlesex, NJ 08846, NDC 64720-128-10

## Reason for recall

Failed Dissolution Specification: Corepharma Inc. is recalling Pyridostigmine Bromide Tablets USP 60 mg due to an out of specification dissolution test generated at the 30 month stability time point.

## Distribution

Nationwide and Puerto Rico

## Key facts

- **Recall number:** D-1079-2014
- **Recalling firm:** Corepharma LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-12-13
- **Report date:** 2014-02-12
- **Termination date:** 2015-01-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Middlesex, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1079-2014

## Citation

> AI Analytics. FDA recall D-1079-2014. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-1079-2014. Source: US FDA. Licensed CC0.

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