Drug recall
Nardil Tablets (Phenelzine Sulfate Tablets, USP), 15 mg, 100 count bottles, Rx Only, PARKE-DAVIS, Div of…
FDA recall event 27720 · Class III · Pfizer Inc
Key facts
| Event ID | 27720 |
|---|---|
| Recall numbers | D-082-4 |
| Recalling firm | Pfizer Inc |
| Product type | Drugs |
| Products | Nardil Tablets (Phenelzine Sulfate Tablets, USP), 15 mg, 100 count bottles, Rx Only, PARKE-DAVIS, Div of Warner-Lambert Co, Morris Plains, NJ 07950 USA, NDC 0071-0270-24. |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Subpotent: (stability) |
| Initiation date | Nov 14, 2003 |
| City | New York |
| Country | United States |
| FEI number | 2416101 |
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