NDC11 42602000201
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 |
|---|---|
| 42602-0002-01 | 42602-0002 |
| 42602-0002-1 | 42602-0002 |
| 42602-002-01 | 42602-002 |
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 |
|---|---|---|---|---|---|---|
| HELIUM | HELIUM | Norco, Inc. | e1d2805c-1ede-4de5-b06e-f5cffc3ffd3c | 2025-08-31 | 42602-002-01 42602-002 42602000201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.