NDC11 00220233041
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 |
|---|---|
| 00220-2330-41 | 00220-2330 |
| 0220-2330-41 | 0220-2330 |
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 |
|---|---|---|---|---|---|---|
| GRATIOLA OFFICINALIS | GRATIOLA OFFICINALIS WHOLE | Boiron | 3a750f92-d3e7-640f-e063-6294a90a73f0 | 2025-07-21 | 0220-2330-41 0220-2330 00220233041 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.