# FDA recall D-0113-2018

> **Advanced Pharma Inc.** · Class I · drug recall initiated 2017-06-09.

## Product

NitroGlycerin 1 mg/10 mL in 5% Dextrose Inj, USP QS 10mL (100 mcg per mL), 10 mL Sterile single dose syringe, packaged in 5 x 5 (TWENTY FIVE) syringes per box, Rx only, Advanced Pharma, 9265 Kirby Dr., Houston, TX  77054, NDC 15082-818-61.

## Reason for recall

Subpotent Drug: found to be below the specification for labeled assay.

## Distribution

Nationwide in the USA to hospitals and medical facilities.

## Key facts

- **Recall number:** D-0113-2018
- **Recalling firm:** Advanced Pharma Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-06-09
- **Report date:** 2017-12-27
- **Termination date:** 2019-04-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Houston, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0113-2018

## Citation

> AI Analytics. FDA recall D-0113-2018. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-0113-2018. Source: US FDA. Licensed CC0.

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