NDC11 31722094901
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 |
|---|---|
| 31722-0949-01 | 31722-0949 |
| 31722-0949-1 | 31722-0949 |
| 31722-949-01 | 31722-949 |
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 AND ACETAMINOPHEN | Camber Pharmaceuticals, Inc. | 42777191-0454-4ccb-8fc3-8b18b0ee43f7 | 2025-08-05 | Boxed warning, Warnings, Adverse reactions | 31722-949-01 31722-949 31722094901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.