NDC11 71753800701
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 |
|---|---|
| 71753-8007-01 | 71753-8007 |
| 71753-8007-1 | 71753-8007 |
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 |
|---|---|---|---|---|---|---|
| Kali Sulphuricum | KALI SULPHURICUM | Ratis, LLC | f0061e89-ff0e-452e-9a9c-ee24020b3e88 | 2023-07-13 | Warnings | 71753-8007-1 71753-8007 71753800701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.