NDC11 42658001001
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 |
|---|---|
| 42658-0010-01 | 42658-0010 |
| 42658-0010-1 | 42658-0010 |
| 42658-010-01 | 42658-010 |
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 |
|---|---|---|---|---|---|---|
| Cladribine | CLADRIBINE | Hisun Pharmaceuticals USA, Inc. | 71c39b37-33b5-42e1-bf4f-93ff751cc7fe | 2025-12-23 | Boxed warning, Warnings, Adverse reactions | 42658-010-01 42658-010 42658001001 |
| Cladribine | CLADRIBINE | Hisun Pharmaceuticals USA, Inc. | f538cba9-001a-4a21-e053-2a95a90a00ec | 2025-01-23 | Boxed warning, Warnings, Adverse reactions | 42658-010 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.