NDC11 00220003543
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 |
|---|---|
| 00220-0035-43 | 00220-0035 |
| 00220-035-43 | 00220-035 |
| 0220-0035-43 | 0220-0035 |
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 |
|---|---|---|---|---|---|---|
| Aconitum napellus | ACONITUM NAPELLUS | Boiron | 840f7e2c-d7a3-d2ac-e053-2991aa0ac04a | 2025-09-10 | 0220-0035-43 0220-0035 00220003543 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.