NDC11 00078081181
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 |
|---|---|
| 00078-0811-81 | 00078-0811 |
| 00078-811-81 | 00078-811 |
| 0078-0811-81 | 0078-0811 |
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 |
|---|---|---|---|---|---|---|
| Sandostatin LAR Depot | OCTREOTIDE ACETATE | Novartis Pharmaceuticals Corporation | d0b7fe9e-7000-4b79-ba3b-291ce92c14f9 | 2025-12-22 | Warnings, Adverse reactions | 0078-0811-81 0078-0811 00078081181 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.