NDC11 65862086005
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 |
|---|---|
| 65862-0860-05 | 65862-0860 |
| 65862-0860-5 | 65862-0860 |
| 65862-860-05 | 65862-860 |
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 | Aurobindo Pharma Limited | b0798337-1a73-415e-8416-613984ce5c65 | 2025-03-04 | Warnings, Adverse reactions | 65862-860-05 65862-860 65862086005 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.