NDC11 70518071803
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 |
|---|---|
| 70518-0718-03 | 70518-0718 |
| 70518-0718-3 | 70518-0718 |
| 70518-718-03 | 70518-718 |
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 |
|---|---|---|---|---|---|---|
| Losartan Potassium | LOSARTAN POTASSIUM | REMEDYREPACK INC. | 25c93638-7016-47d2-a57c-e4a5245ca41b | 2026-06-30 | Boxed warning, Warnings, Adverse reactions | 70518-0718-3 70518-0718 70518071803 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.