Drug recall
PREMARIN Tablets, 0.9 mg (conjugated estrogens tablets, USP), 100 tablet bottles, Rx Only, Ayerst Laboratories…
FDA recall event 25672 · Class III · Robins, A.H./Division of American Home Products
Key facts
| Event ID | 25672 |
|---|---|
| Recall numbers | D-183-3, D-184-3 |
| Recalling firm | Robins, A.H./Division of American Home Products |
| Product type | Drugs |
| Products | PREMARIN Tablets, 0.9 mg (conjugated estrogens tablets, USP), 100 tablet bottles, Rx Only, Ayerst Laboratories inc, A Wyeth-Ayerst Company, Philadelphia, PA 19101, NDC #0046-0864-81., Premarin tablets, 1.25 mg, (conjugated estrogens tablets, USP), 5,000 count bottles, Rx Only, Ayerst Laboratories Inc, A Wyeth-Ayerst Company, Philadelphia, PA 19101, NDC#0046-0866-95. |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Dissolution Failure: 5 hour time point |
| Initiation date | Feb 21, 2003 |
| 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