NDC11 00054084363
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 |
|---|---|
| 00054-0843-63 | 00054-0843 |
| 00054-843-63 | 00054-843 |
| 0054-0843-63 | 0054-0843 |
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 |
|---|---|---|---|---|---|---|
| HYDROCODONE BITARTRATE AND ACETAMINOPHEN | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | Hikma Pharmaceuticals USA Inc. | 995a6cc7-8b72-4d35-b3b4-8c5752438fb7 | 2026-07-28 | Boxed warning, Warnings, Adverse reactions | 0054-0843-63 0054-0843 00054084363 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.