NDC11 43742166401

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
43742-1664-01	43742-1664
43742-1664-1	43742-1664

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	CEANOTHUS AMERICANUS, ARGENTUM NITRICUM, CONDURANGO, HYDRASTIS CANADENSIS, MOMORDICA BALSAMINA, PULSATILLA (PRATENSIS), BILE DUCT (SUIS), COLON (SUIS), DUODENUM (SUIS), ESOPHAGUS (SUIS), EYE (SUIS), GALLBLADDER (SUIS), ILEUM (SUIS), INTESTINE (SUIS), IPECACUANHA, JEJUNUM (SUIS), KALI BICHROMICUM, LUNG (SUIS), MUCOSA NASALIS SUIS, NATRUM OXALACETICUM, ORAL MUCOSA (SUIS), PANCREAS SUIS, PHOSPHORUS, RECTAL MUCOSA (SUIS), STOMACH (SUIS), SULPHUR, VERATRUM ALBUM, MANNOSE, ANACARDIUM ORIENTALE, KREOSOTUM,	Deseret Biologicals, Inc.	bae2c721-44e8-4f88-92da-66e8ae03ada0	2026-05-06	Warnings	Exact identifier ndc (package): 43742-1664-1 ndc (product): 43742-1664 ndc11 (package): 43742166401

Reported adverse events (FAERS/openFDA)#

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