# FDA recall D-737-2014

> **Greenstone Llc** · Class II · drug recall initiated 2013-11-01.

## Product

Nifedipine, extended-release tablets, 90mg 100 count blister pack,  Rx only, Distributed by: GREENSTONE LLC, Pespack, NJ,07977, NDC 59762-6692-8

## Reason for recall

Labeling: Incorrect or Missing Lot and/or Exp Date: Greenstone LLC is recalling  Nifedipine Extended Release tablets (90mg). The expiration date on the package is 48 months instead of 36 months.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-737-2014
- **Recalling firm:** Greenstone Llc
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-11-01
- **Report date:** 2014-01-22
- **Termination date:** 2015-06-05

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-737-2014

## Citation

> AI Analytics. FDA recall D-737-2014. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-737-2014. Source: US FDA. Licensed CC0.

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