NDC11 71921025036
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 |
|---|---|
| 71921-0250-36 | 71921-0250 |
| 71921-250-36 | 71921-250 |
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 |
|---|---|---|---|---|---|---|
| Lofexidine | LOFEXIDINE | Florida Pharmaceutical Products, LLC | ce4488e2-842c-45ba-aca7-075a900e2a1c | 2026-05-21 | Warnings, Adverse reactions | 71921-250-36 71921-250 71921025036 |