NDC11 43857013601
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 |
|---|---|
| 43857-0136-01 | 43857-0136 |
| 43857-0136-1 | 43857-0136 |
| 43857-136-01 | 43857-136 |
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 |
|---|---|---|---|---|---|---|
| Nephroplex | BERBERIS VULGARIS, HYDRANGEA ARBORESCENS, PETROSELINUM SATIVUM, SOLIDAGO VIRGAUREA, UVA URSI, RUBIA TINCTORUM, GLUTATHIONE, KIDNEY (SUIS), BRYONIA (ALBA), EUPATORIUM PURPUREUM, MERCURIUS CORROSIVUS | BioActive Nutritional, Inc. | 56a0820a-5f10-4e31-ac67-4ecec164b733 | 2026-09-03 | Warnings | 43857-0136-1 43857-0136 43857013601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.