Drug recall
Alprazolam Extended-Release Tablets, USP, 3 mg, 60-count tablets per bottle, Rx only, Manufactured by: Actavis…
FDA recall event 67518 · Class II · Actavis Elizabeth LLC
Key facts
| Event ID | 67518 |
|---|---|
| Recall numbers | D-1091-2014 |
| Recalling firm | Actavis Elizabeth LLC |
| Product type | Drugs |
| Products | Alprazolam Extended-Release Tablets, USP, 3 mg, 60-count tablets per bottle, Rx only, Manufactured by: Actavis Elizabeth LLC, 200 Elmora Avenue, Elizabeth, NJ 07207, NDC 0228-3086-06, UPC 3… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Failed Dissolution Specifications: Product did not meet specification requirements for dissolution. |
| Initiation date | Feb 4, 2014 |
| Report date | Mar 12, 2014 |
| Termination date | Jan 22, 2015 |
| City | Elizabeth |
| State | NJ |
| Country | United States |
| FEI number | 2211563 |
At a glance
- 1–9 Products in this recall
- 10–99 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: