NDC11 24338015020
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 24338-0150-20 | 24338-0150 |
| 24338-150-20 | 24338-150 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| TRIPTODUR | TRIPTORELIN | Azurity Pharmaceuticals, Inc. | f41380e7-b830-432d-a5f5-a872932f107e | 2025-09-14 | Warnings, Adverse reactions | 24338-150-20 24338-150 24338015020 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.