Drug recall
CENESTIN (synthetic conjugated estrogens, A)Tablets, 0.625 mg., Rx only, 1000 count bottles, Duramed…
FDA recall event 29606 · Class III · Barr Pharmaceuticals Inc
Key facts
| Event ID | 29606 |
|---|---|
| Recall numbers | D-250-4 |
| Recalling firm | Barr Pharmaceuticals Inc |
| Product type | Drugs |
| Products | CENESTIN (synthetic conjugated estrogens, A )Tablets, 0.625 mg., Rx only, 1000 count bottles, Duramed Pharmaceuticals, Inc., Cincinnati, OH 45213, NDC 51285-442-05 |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Stability Failure: 36 month stability failure due to excessive moisture |
| Initiation date | Jul 26, 2004 |
| City | Cincinnati |
| Country | United States |
| FEI number | 1526814 |
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