NDC11 43742254301

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 NDC	Product root
43742-2543-01	43742-2543
43742-2543-1	43742-2543

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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Matrix Support	ANACARDIUM ORIENTALE, ARGENTUM NITRICUM, BILE DUCT (SUIS), CEANOTHUS AMERICANUS, COLON (SUIS), CONDURANGO, DUODENUM (SUIS), DYSENTERY BACILLUS, ESOPHAGUS (SUIS), EYE (SUIS), GALLBLADDER (SUIS), HYDRASTIS CANADENSIS, ILEUM (SUIS), INTESTINE (SUIS), IPECACUANHA, JEJUNUM (SUIS), KALI BICHROMICUM, KREOSOTUM, LACHESIS MUTUS, LUNG (SUIS), MANNOSE, MOMORDICA BALSAMINA, MUCOSA NASALIS SUIS, NATRUM OXALACETICUM, ORAL MUCOSA (SUIS), OXALIS ACETOSELLA, PANCREAS SUIS, PHOSPHORUS, PULSATILLA (PRATENSIS),	Deseret Biologicals, Inc.	9b44f9d1-1ec6-4b01-8992-508a5fb15aae	2026-06-15	Warnings	Exact identifier ndc (package): 43742-2543-1 ndc (product): 43742-2543 ndc11 (package): 43742254301

Reported adverse events (FAERS/openFDA)#

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