NDC11 43742209201

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
43742-2092-0143742-2092
43742-2092-143742-2092

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
ProstatePETROSELINUM SATIVUM, POPULUS TREMULOIDES, SABAL SERRULATA, CHIMAPHILA UMBELLATA, ADENOSINUM TRIPHOSPHORICUM DINATRUM, EQUOL, KREOSOTUM, NADIDUM, TESTOSTERONE, PROSTATE (SUIS), SUCCINICUM ACIDUM, HEPAR SULPHURIS CALCAREUM, CONIUM MACULATUM, PROTEUS (MIRABILIS), PROTEUS (VULGARIS)Deseret Biologicals, Inc.776af24a-d9c1-4ecd-8e5d-0ab32c60e7152024-08-19WarningsExact identifier
ndc (package): 43742-2092-1
ndc (product): 43742-2092
ndc11 (package): 43742209201

Reported adverse events (FAERS/openFDA)#

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