Drug recall
Greenstone brand cabergoline tablets, 0.5 mg, 8 tablets per bottle, RX only, NDC 59762-0100-1, Greenstone…
FDA recall event 35360 · Class III · Greenstone Ltd.
Key facts
| Event ID | 35360 |
|---|---|
| Recall numbers | D-247-6 |
| Recalling firm | Greenstone Ltd. |
| Product type | Drugs |
| Products | Greenstone brand cabergoline tablets, 0.5 mg, 8 tablets per bottle, RX only, NDC 59762-0100-1, Greenstone Ltd., Peapack, NJ 07977 |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Product will not meet established potency and impurity specifications throughout its labeled shelf life. |
| Initiation date | Apr 27, 2006 |
| City | Peapack |
| Country | United States |
| FEI number | 3004959301 |
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