Drug recall
Premarin (conjugated estrogens) tablets, USP, 0.625 mg; Rx only,Wyeth Pharmaceuticals, Inc., Philadelphia, PA…
FDA recall event 30658 · Class III · Richmond Division of Wyeth
Key facts
| Event ID | 30658 |
|---|---|
| Recall numbers | D-078-5 |
| Recalling firm | Richmond Division of Wyeth |
| Product type | Drugs |
| Products | Premarin (conjugated estrogens) tablets, USP, 0.625 mg; Rx only,Wyeth Pharmaceuticals, Inc., Philadelphia, PA 19101; 1000 tablet bottles-NDC 0046-0867-91; 5000 tablet bottles- NDC 0046-0867-95. |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Dissolution Failure |
| Initiation date | Dec 10, 2004 |
| City | Richmond |
| Country | United States |
| FEI number | 1110584 |
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