NDC11 15631002707
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 |
|---|---|
| 15631-0027-07 | 15631-0027 |
| 15631-0027-7 | 15631-0027 |
| 15631-027-07 | 15631-027 |
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 |
|---|---|---|---|---|---|---|
| AMMONIUM CARBONICUM | AMMONIUM CARBONICUM | Rxhomeo Private Limited d.b.a. Rxhomeo, Inc | 4a812041-45e2-4f26-b0c7-670aa7cdcdb0 | 2021-10-08 | Warnings | 15631-0027-7 15631-0027 15631002707 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.