NDC11 70436012380
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 |
|---|---|
| 70436-0123-80 | 70436-0123 |
| 70436-123-80 | 70436-123 |
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 |
|---|---|---|---|---|---|---|
| gadoterate meglumine | GADOTERATE MEGLUMINE | Slate Run Pharmaceuticals, LLC | 85404ca7-dbe7-4d06-b30c-4368dcd33b0b | 2025-04-16 | Boxed warning, Warnings, Adverse reactions | 70436-123 |
| gadoterate meglumine | GADOTERATE MEGLUMINE | Slate Run Pharmaceuticals, LLC | b4159c07-b114-4256-b9a9-e6af811704fa | 2025-04-16 | Boxed warning, Warnings, Adverse reactions | 70436-123-80 70436-123 70436012380 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.