NDC11 00220396841
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 |
|---|---|
| 00220-3968-41 | 00220-3968 |
| 0220-3968-41 | 0220-3968 |
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 |
|---|---|---|---|---|---|---|
| Pertussinum | HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED | Boiron | 875c1597-da1f-46df-e053-2995a90a0bd0 | 2023-11-14 | 0220-3968-41 0220-3968 00220396841 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.