NDC11 55681034303
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 |
|---|---|
| 55681-0343-03 | 55681-0343 |
| 55681-0343-3 | 55681-0343 |
| 55681-343-03 | 55681-343 |
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 |
|---|---|---|---|---|---|---|
| Famotidine | FAMOTIDINE | TWIN MED LLC | 795afb99-a3f4-4ffc-a905-2f84f3d86e4c | 2026-06-16 | Warnings | 55681-343-03 55681-343 55681034303 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.