BuPROPion HCL Tablets — Class III drug recall D-0928-2017
Terminated recall by Mckesson Packaging Services, reported 2017-07-05, distributed nationwide. Failed Moisture Limits: Product tested out-of-specification for moisture content.
| Recall number | D-0928-2017 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mckesson Packaging Services, Concord, NC, United States |
| Recall initiated | 2017-05-30 |
| Classified | 2017-06-29 |
| Reported by FDA | 2017-07-05 |
| Terminated | 2020-02-06 |
| Distributed | Nationwide (US) |
| Quantity | 942 cartons |
| NDC | 63739-0706-10 |
| Lot numbers | 0113148, 0113149, 0113150, 0113636, 0114513, 04/18, 06/18, 10/18 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0928-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.