NDC11 70954090910
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 |
|---|---|
| 70954-0909-10 | 70954-0909 |
| 70954-909-10 | 70954-909 |
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 | ANI Pharmaceuticals, Inc. | 335e26bf-b236-46d6-81cf-2879e5f3b1d9 | 2024-09-05 | Warnings, Adverse reactions | 70954-909-10 70954-909 70954090910 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.