NDC11 00220026941
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 |
|---|---|
| 00220-0269-41 | 00220-0269 |
| 00220-269-41 | 00220-269 |
| 0220-0269-41 | 0220-0269 |
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 |
|---|---|---|---|---|---|---|
| Ammonium phosphoricum | AMMONIUM PHOSPHATE DIBASIC | Boiron | 13f29305-9e6c-7570-e063-6394a90a908d | 2024-03-18 | 0220-0269-41 0220-0269 00220026941 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.