Drug recall
Premarin (conjugated estrogens tablets USP), 0.3 mg, 1,000 tablet bottles, Rx, NDC 0046-0868-91. Firm on…
FDA recall event 31575 · Class III · Richmond Division of Wyeth
Key facts
| Event ID | 31575 |
|---|---|
| Recall numbers | D-188-5, D-189-5 |
| Recalling firm | Richmond Division of Wyeth |
| Product type | Drugs |
| Products | Premarin (conjugated estrogens tablets USP), 0.3 mg, 1,000 tablet bottles, Rx, NDC 0046-0868-91. Firm on label: Ayerst Laboratories, A Wyeth-Ayerst Company, Philadelphia, PA 19101, Premarin (conjugated estrogens tablets USP), 0.625 mg, 1,000 tablet bottles, Rx, NDC 0046-0867-91. Firm on label: Wyeth Pharmaceuticals Inc., Philadelphia, PA 19101 |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Dissolution failures. |
| Initiation date | Apr 4, 2005 |
| 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