Drug recall
ChlorproMAZINE Hydrochloride Tablets, USP, 50 mg, 100 and 1000 count bottles, Rx only Manufactured by…
FDA recall event 38443 · Class III · Upsher Smith Laboratories, Inc.
Key facts
| Event ID | 38443 |
|---|---|
| Recall numbers | D-952-2007 |
| Recalling firm | Upsher Smith Laboratories, Inc. |
| Product type | Drugs |
| Products | ChlorproMAZINE Hydrochloride Tablets, USP, 50 mg, 100 and 1000 count bottles, Rx only Manufactured by UPSHER-SMITH LABORATORIES, INC. Minneapolis, MN 55447 ----- NDC 0832-0302-00 and 0832-0302-01 |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Upsher-Smith Chlorpromazine Hydrochloride 50 mg tablets, USP may contain an illegible or missing imprint on tablet |
| Initiation date | Jul 23, 2007 |
| Termination date | Jan 2, 2009 |
| City | Maple Grove |
| State | MN |
| Country | United States |
| FEI number | 3004106442 |
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