NDC11 32909018702
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 |
|---|---|
| 32909-0187-02 | 32909-0187 |
| 32909-0187-2 | 32909-0187 |
| 32909-187-02 | 32909-187 |
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 |
|---|---|---|---|---|---|---|
| E-Z-Paque | BARIUM SULFATE | E-Z-EM Canada Inc | 2ecea1ab-66c8-4eb0-8503-6d6b41b51328 | 2026-04-15 | Warnings, Adverse reactions | 32909-187-02 32909-187 32909018702 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.