NDC11 10167020001
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 |
|---|---|
| 10167-0200-01 | 10167-0200 |
| 10167-0200-1 | 10167-0200 |
| 10167-200-01 | 10167-200 |
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 |
|---|---|---|---|---|---|---|
| NITROUS OXIDE | NITROUS OXIDE | Air Source Industries | eebd56c1-4ab3-409b-9767-e54dc42f2fce | 2024-10-06 | 10167-200-01 10167-200 10167020001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.