NDC11 21221000203
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 |
|---|---|
| 21221-0002-03 | 21221-0002 |
| 21221-0002-3 | 21221-0002 |
| 21221-002-03 | 21221-002 |
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 |
|---|---|---|---|---|---|---|
| Oxygen | OXYGEN | General Cryogenic Technologies LLC | c071ca0b-a330-4579-a1b8-d4b4c5824a09 | 2025-11-21 | 21221-002-03 21221-002 21221000203 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.