Drug recall
BuPROPion HCL Tablets, USP, 75 mg, packaged as UD 100 tablets (10x10), Rx Only, Mfg by: Sandoz Inc., 508…
FDA recall event 77411 · Class III · Mckesson Packaging Services
Key facts
| Event ID | 77411 |
|---|---|
| Recall numbers | D-0928-2017 |
| Recalling firm | Mckesson Packaging Services |
| Product type | Drugs |
| Products | 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 |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Failed Moisture Limits: Product tested out-of-specification for moisture content. |
| Initiation date | May 30, 2017 |
| Report date | Jul 5, 2017 |
| Termination date | Feb 6, 2020 |
| City | Concord |
| State | NC |
| Country | United States |
| FEI number | 3000206187 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: