NDC11 00220506541
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 |
|---|---|
| 00220-5065-41 | 00220-5065 |
| 0220-5065-41 | 0220-5065 |
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 |
|---|---|---|---|---|---|---|
| TUBERCULINUM RESIDUUM | TUBERCULINUM RESIDUUM | Boiron | eb02f516-8682-415d-e053-2995a90a5f75 | 2023-01-18 | 0220-5065-41 0220-5065 00220506541 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.