NDC11 63020072520
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 |
|---|---|
| 63020-0725-20 | 63020-0725 |
| 63020-725-20 | 63020-725 |
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 |
|---|---|---|---|---|---|---|
| MIMRYLO | RUSFERTIDE | Takeda Pharmaceuticals America, Inc. | 101aff01-31ed-4841-a8b6-0a5a8503189b | 2026-08-28 | Warnings, Adverse reactions | 63020-725-20 63020-725 63020072520 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.