NDC11 70010019009
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 |
|---|---|
| 70010-0190-09 | 70010-0190 |
| 70010-0190-9 | 70010-0190 |
| 70010-190-09 | 70010-190 |
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 |
|---|---|---|---|---|---|---|
| pantoprazole sodium | PANTOPRAZOLE SODIUM | Granules Pharmaceuticals Inc. | 8f2fb647-15bc-41cb-84a4-02e956e614fc | 2026-04-06 | Warnings, Adverse reactions | 70010-190-09 70010-190 70010019009 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.