NDC11 00406052201
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 |
|---|---|
| 00406-0522-01 | 00406-0522 |
| 00406-0522-1 | 00406-0522 |
| 00406-522-01 | 00406-522 |
| 0406-0522-01 | 0406-0522 |
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 |
|---|---|---|---|---|---|---|
| OXYCODONE AND ACETAMINOPHEN | OXYCODONE HYDROCHLORIDE AND ACETAMINOPHEN | SpecGx LLC | f2137f1a-b49a-40bd-97ac-cd6b36e295f4 | 2026-07-27 | Boxed warning, Warnings, Adverse reactions | 0406-0522-01 0406-0522 00406052201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.