NDC11 15631031207
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 |
|---|---|
| 15631-0312-07 | 15631-0312 |
| 15631-0312-7 | 15631-0312 |
| 15631-312-07 | 15631-312 |
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 |
|---|---|---|---|---|---|---|
| NATRUM SULPHURICUM | NATRUM SULPHURICUM | Rxhomeo Private Limited d.b.a. Rxhomeo, Inc | d4e87869-f21c-4324-97f4-d4b52ba12fd3 | 2021-10-06 | Warnings | 15631-0312-7 15631-0312 15631031207 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.