NDC11 71205060330
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 |
|---|---|
| 71205-0603-30 | 71205-0603 |
| 71205-603-30 | 71205-603 |
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 | Proficient Rx LP | 0f5eb1b4-ad4b-4782-8d3d-cd33f9c5be7d | 2022-04-01 | Warnings, Adverse reactions | 71205-603-30 71205-603 71205060330 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.