NDC11 65862072130
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 |
|---|---|
| 65862-0721-30 | 65862-0721 |
| 65862-721-30 | 65862-721 |
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 |
|---|---|---|---|---|---|---|
| Rabeprazole Sodium | RABEPRAZOLE SODIUM | Aurobindo Pharma Limited | d11c3211-b4d4-4893-8c1c-b8fb6d0a0b89 | 2024-02-28 | Warnings, Adverse reactions | 65862-721-30 65862-721 65862072130 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.