NDC11 51012000203
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 |
|---|---|
| 51012-0002-03 | 51012-0002 |
| 51012-0002-3 | 51012-0002 |
| 51012-002-03 | 51012-002 |
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 |
|---|---|---|---|---|---|---|
| NITROGEN | NITROGEN | Gilmore Liquid Air Co. | b9c7597b-3371-487e-9f63-eaf97660f364 | 2024-10-21 | 51012-002-03 51012-002 51012000203 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.