NDC11 43742219801

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 table
Package NDCProduct root
43742-2198-0143742-2198
43742-2198-143742-2198

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.

Matched openFDA labels page 1 of 1 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
NausiaARSENICUM ALBUM, BRYONIA (ALBA), CADMIUM SULPHURATUM, COCCULUS INDICUS, COLCHICUM AUTUMNALE, CONIUM MACULATUM, CYCLAMEN EUROPAEUM, EUPHORBIA COROLLATA, FERRUM METALLICUM, IPECACUANHA, IRIS VERSICOLOR, LAC DEFLORATUM, LACTICUM ACIDUM, NUX VOMICA, PETROLEUM, PULSATILLA (PRATENSIS), SEPIA, TABACUM, THERIDION, ZINGIBER OFFICINALEDeseret Biologicals, Inc.025ed334-29dd-4519-b9f6-cf560e73c2942024-09-23WarningsExact identifier
ndc (package): 43742-2198-1
ndc (product): 43742-2198
ndc11 (package): 43742219801

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.