NDC 71052-062-15 - Trilostane
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 71052-062
- Requested NDC
- 71052-062-15
- Package NDCs from labels
- 71052-062-10, 71052-062-15, 71052-062-00, 71052-062-05, 71052-062-01
- Manufacturer
- Darmerica, LLC
- Effective date
- 2021-04-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Trilostane - Darmerica, LLC | Darmerica, LLC | 2021-04-14 | BULK INGREDIENT |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.