NDC11 24338001801
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 |
|---|---|
| 24338-0018-01 | 24338-0018 |
| 24338-0018-1 | 24338-0018 |
| 24338-018-01 | 24338-018 |
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 |
|---|---|---|---|---|---|---|
| MYHIBBIN | MYCOPHENOLATE MOFETIL | Azurity Pharmaceuticals, Inc. | d9af72d6-7b3e-4c08-94b9-1d8b499cb7f9 | 2026-04-01 | Boxed warning, Warnings, Adverse reactions | 24338-018-01 24338-018 24338001801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.