# FDA recall D-0928-2017

> **Mckesson Packaging Services** · Class III · drug recall initiated 2017-05-30.

## Product

BuPROPion HCL Tablets, USP, 75 mg, packaged as UD 100 tablets (10x10), Rx Only, Mfg by: Sandoz Inc., 508 Carnegie Center, Suite 400, Princeton, NJ 08805, NDC: 63739-706-10

## Reason for recall

Failed Moisture Limits: Product tested out-of-specification for moisture content.

## Distribution

Nationwide in the US

## Key facts

- **Recall number:** D-0928-2017
- **Recalling firm:** Mckesson Packaging Services
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-05-30
- **Report date:** 2017-07-05
- **Termination date:** 2020-02-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Concord, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0928-2017

## Citation

> AI Analytics. FDA recall D-0928-2017. Retrieved 2026-07-19 from https://api.ai-analytics.org/recall/D-0928-2017. Source: US FDA. Licensed CC0.

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