NDC11 70121246101
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 |
|---|---|
| 70121-2461-01 | 70121-2461 |
| 70121-2461-1 | 70121-2461 |
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 |
|---|---|---|---|---|---|---|
| PEMRYDI RTU | PEMETREXED DISODIUM | Amneal Pharmaceuticals LLC | 0f006b06-ab85-423d-ba0c-dfc3fc25844e | 2025-07-08 | Warnings, Adverse reactions | 70121-2461-1 70121-2461 70121246101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.