NDC11 00049011428
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 |
|---|---|
| 00049-0114-28 | 00049-0114 |
| 00049-114-28 | 00049-114 |
| 0049-0114-28 | 0049-0114 |
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 |
|---|---|---|---|---|---|---|
| ERAXIS | ANIDULAFUNGIN | Roerig | a88d9010-55fb-4a02-baff-042cd27688ea | 2025-08-19 | Warnings, Adverse reactions | 0049-0114-28 0049-0114 00049011428 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.