Drug recall
Alprazolam Extended-Release Tablets, 3mg, Rx only, packaged in 60 count plastic (HDPE) bottles, Sandoz, Inc…
FDA recall event 46848 · Class II · Sandoz Inc
Key facts
| Event ID | 46848 |
|---|---|
| Recall numbers | D-166-2008 |
| Recalling firm | Sandoz Inc |
| Product type | Drugs |
| Products | Alprazolam Extended-Release Tablets, 3mg, Rx only, packaged in 60 count plastic (HDPE) bottles, Sandoz, Inc., Princeton, NJ 08540 --- NDC 0185-0198-60 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Failed Dissolution Specification (6 month stability) |
| Initiation date | Feb 11, 2008 |
| Termination date | Jun 8, 2009 |
| City | Princeton |
| State | NJ |
| Country | United States |
| FEI number | 3005274779 |
At a glance
- 1–9 Products in this recall
- None 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