Drug recall
ANASTROZOLE tablets, 1 mg, 30 Tablets per HDPE Bottle, Rx only, Manufactured for APP Pharmaceuticals, LLC…
FDA recall event 56681 · Class III · APP Pharmaceuticals LLC
Key facts
| Event ID | 56681 |
|---|---|
| Recall numbers | D-906-2010 |
| Recalling firm | APP Pharmaceuticals LLC |
| Product type | Drugs |
| Products | ANASTROZOLE tablets, 1 mg, 30 Tablets per HDPE Bottle, Rx only, Manufactured for APP Pharmaceuticals, LLC, Schaumburg, IL 60173, Made in India; NDC #63323-129-30 |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Presence of Foreign Tablets/Capsules; A potential for some foreign tablets of Letrozole to be in bottles of anastrozole tablets 1 mg |
| Initiation date | Sep 1, 2010 |
| Termination date | Jun 30, 2011 |
| City | Schaumburg |
| State | IL |
| Country | United States |
| FEI number | 3002733956 |
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