NDC11 27854070101
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 |
|---|---|
| 27854-0701-01 | 27854-0701 |
| 27854-0701-1 | 27854-0701 |
| 27854-701-01 | 27854-701 |
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 |
|---|---|---|---|---|---|---|
| Ana-Dent PAIN RELIEF | NAPROXEN SODIUM | Belmora LLC | 04721306-2850-4e0a-9dd9-7cabb575f3c7 | 2020-05-18 | Warnings | 27854-701-01 27854-701 27854070101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.