NDC11 00220077041
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 |
|---|---|
| 00220-0770-41 | 00220-0770 |
| 00220-770-41 | 00220-770 |
| 0220-0770-41 | 0220-0770 |
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 |
|---|---|---|---|---|---|---|
| Baptisia tinctoria | BAPTISIA TINCTORIA ROOT | Boiron | 84f16e5d-25d8-371e-e053-2991aa0a50e1 | 2023-11-09 | 0220-0770-41 0220-0770 00220077041 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.