NDC11 70518422703
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 |
|---|---|
| 70518-4227-03 | 70518-4227 |
| 70518-4227-3 | 70518-4227 |
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 |
|---|---|---|---|---|---|---|
| Lithium | LITHIUM | REMEDYREPACK INC. | be1346df-4a39-45e8-874b-e2a496847fd5 | 2026-08-31 | Boxed warning, Warnings, Adverse reactions | 70518-4227-3 70518-4227 70518422703 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.