NDC11 70183012503
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 |
|---|---|
| 70183-0125-03 | 70183-0125 |
| 70183-0125-3 | 70183-0125 |
| 70183-125-03 | 70183-125 |
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 |
|---|---|---|---|---|---|---|
| Xermelo | TELOTRISTAT ETHYL | Lexicon Pharmaceuticals, Inc. | f9108ac3-ca6e-4faf-9d04-953abb64d072 | 2025-10-01 | Warnings, Adverse reactions | 70183-125 |
| Xermelo | TELOTRISTAT ETHYL | Lexicon Pharmaceuticals, Inc. | f11c21f8-f725-445e-b38e-1e4c5b05bcc6 | 2025-10-01 | Warnings, Adverse reactions | 70183-125-03 70183-125 70183012503 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.