NDC11 85816508801
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 |
|---|---|
| 85816-5088-01 | 85816-5088 |
| 85816-5088-1 | 85816-5088 |
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 |
|---|---|---|---|---|---|---|
| BM Ruta Graveolens | RUTA GRAVEOLENS | BM Private Limited | 38e29eff-6f5f-3bbf-e063-6394a90aa9c6 | 2025-07-01 | Warnings | 85816-5088-1 85816-5088 85816508801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.