NDC11 43742211401
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 |
|---|---|
| 43742-2114-01 | 43742-2114 |
| 43742-2114-1 | 43742-2114 |
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 |
|---|---|---|---|---|---|---|
| Systemic Drainage | ALFALFA, AVENA SATIVA, BERBERIS VULGARIS, CHELIDONIUM MAJUS, CITRUS LIMONUM, GALIUM APARINE, GLYCYRRHIZA GLABRA, HEPAR SUIS, INTESTINE (SUIS), KIDNEY (SUIS), LACTICUM ACIDUM, LUNG (SUIS), LYMPH NODE (SUIS), MAGNESIUM GLUCONATE DIHYDRICUM, NUX VOMICA, POTASSIUM GLUCONATE, SARCOLACTICUM ACIDUM, SCHISANDRA CHINENSIS, SOLIDAGO VIRGAUREA, TABACUM, TARAXACUM OFFICINALE, TYLOPHORA ASTHMATICA, UVA-URSI, ZINCUM GLUCONICUM. | Deseret Biologicals, Inc. | 0c3e924e-f0ea-470e-971f-c4c0b8eef146 | 2024-02-19 | Warnings | 43742-2114-1 43742-2114 43742211401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.