Drug recall
Tegretol tablets (Carbamazepine USP), 200 mg, 1000 tablet bottles, Rx only, Novartis Pharmaceuticals…
FDA recall event 27130 · Class II · Novartis Pharmaceuticals Corp.
Key facts
| Event ID | 27130 |
|---|---|
| Recall numbers | D-008-4 |
| Recalling firm | Novartis Pharmaceuticals Corp. |
| Product type | Drugs |
| Products | Tegretol tablets (Carbamazepine USP), 200 mg, 1000 tablet bottles, Rx only, Novartis Pharmaceuticals Corporation, East Hanover, New Jersey 07936, NDC 0083-0027-40 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Dissolution failure; stability (at 30-months) |
| Initiation date | Sep 2, 2003 |
| City | Suffern |
| Country | United States |
| FEI number | 2416082 |
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