NDC11 00088210201
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 |
|---|---|
| 00088-2102-01 | 00088-2102 |
| 00088-2102-1 | 00088-2102 |
| 0088-2102-01 | 0088-2102 |
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 |
|---|---|---|---|---|---|---|
| Priftin | RIFAPENTINE | sanofi-aventis U.S. LLC | 3a64fb70-b85e-43d9-8bcd-7e893f568ae1 | 2026-02-06 | Warnings, Adverse reactions | 0088-2102-01 0088-2102 00088210201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.