NDC11 71288016750
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 |
|---|---|
| 71288-0167-50 | 71288-0167 |
| 71288-167-50 | 71288-167 |
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 |
|---|---|---|---|---|---|---|
| Pemetrexed | PEMETREXED DISODIUM | Meitheal Pharmaceuticals Inc. | e0d000a3-b9d2-4fa9-9591-f7acb077481d | 2025-11-17 | Warnings, Adverse reactions | 71288-167 |
| Pemetrexed | PEMETREXED DISODIUM | Meitheal Pharmaceuticals Inc. | 1ceacc3e-f555-489b-8b16-2baa58b2f5a5 | 2024-04-19 | Warnings, Adverse reactions | 71288-167-50 71288-167 71288016750 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.