NDC 76346-025 - Lifyorli
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
- 76346-025
- Package NDCs from labels
- 76346-025-01
- Manufacturer
- Corcept Therapeutics Incorporated
- Effective date
- 2026-03-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Lifyorli - Corcept Therapeutics Incorporated | Corcept Therapeutics Incorporated | 2026-03-26 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 76346-025-01 | Lifyorli | 1 in 1 PACKAGE, COMBINATION | CAPSULE | 1 | 25 mg | 1 |
| 76346-025-01 | Lifyorli | 1 in 1 PACKAGE, COMBINATION | CAPSULE | 2 | 25 mg | 1 |
| 76346-025-01 | Lifyorli | 1 in 1 PACKAGE, COMBINATION | CAPSULE | 3 | 25 mg | 1 |
| 76346-025-01 | Lifyorli | 1 in 1 PACKAGE, COMBINATION | CAPSULE | 6 | 25 mg | 1 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.