NDC11 50063000405
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 |
|---|---|
| 50063-0004-05 | 50063-0004 |
| 50063-0004-5 | 50063-0004 |
| 50063-004-05 | 50063-004 |
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 |
|---|---|---|---|---|---|---|
| Air | AIR | Andy-Oxy Co., Inc. | 60cc80bb-8fe9-fd31-e053-2991aa0a4895 | 2025-10-30 | 50063-004-05 50063-004 50063000405 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.