Drug recall
Terazosin HCl Capsules, 5 mg, 1000 count bottles, Rx Only, Manufactured by: Cadista Pharmaceuticals Inc…
FDA recall event 54348 · Class III · Cadista Pharmaceuticals Inc.
Key facts
| Event ID | 54348 |
|---|---|
| Recall numbers | D-334-2010 |
| Recalling firm | Cadista Pharmaceuticals Inc. |
| Product type | Drugs |
| Products | Terazosin HCl Capsules, 5 mg, 1000 count bottles, Rx Only, Manufactured by: Cadista Pharmaceuticals Inc., Salisbury, MD 21801, USA; NDC 59746-385-10 |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Pharmaceutical may have been packaged with two dosage strengths of the same drug. |
| Initiation date | May 4, 2009 |
| Termination date | Mar 29, 2010 |
| City | Salisbury |
| State | MD |
| Country | United States |
| FEI number | 1000513046 |
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