NDC11 60505455203
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 |
|---|---|
| 60505-4552-03 | 60505-4552 |
| 60505-4552-3 | 60505-4552 |
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 |
|---|---|---|---|---|---|---|
| Ambrisentan | AMBRISENTAN | Apotex Corp. | 291a782a-77e1-8a8e-e1c8-2626f305c2b7 | 2026-09-03 | Boxed warning, Warnings, Adverse reactions | 60505-4552-3 60505-4552 60505455203 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.