Drug recall
GREENSTONE BRAND, Azithromycin Tablets 500 mg, Rx only, 30 Tablets,Distributed by: Greenstone Ltd., Peapack…
FDA recall event 50913 · Class II · Pfizer Inc
Key facts
| Event ID | 50913 |
|---|---|
| Recall numbers | D-202-2009 |
| Recalling firm | Pfizer Inc |
| Product type | Drugs |
| Products | GREENSTONE BRAND, Azithromycin Tablets 500 mg, Rx only, 30 Tablets,Distributed by: Greenstone Ltd., Peapack, NJ 07977 ---- NDC 59762-3070-2 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Failed Dissolution Specifications; stability |
| Initiation date | Dec 29, 2008 |
| Termination date | Sep 19, 2012 |
| City | New York |
| State | NY |
| Country | United States |
| FEI number | 2416101 |
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