NDC11 60687012301
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 |
|---|---|
| 60687-0123-01 | 60687-0123 |
| 60687-0123-1 | 60687-0123 |
| 60687-123-01 | 60687-123 |
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 |
|---|---|---|---|---|---|---|
| Lansoprazole | LANSOPRAZOLE | American Health Packaging | dee80a19-e514-41e6-9153-c959699d97b1 | 2025-01-07 | Warnings, Adverse reactions | 60687-123-01 60687-123 60687012301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.