NDC11 43742226501

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
43742-2265-01	43742-2265
43742-2265-1	43742-2265

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
Heart Small Intestine Meridian Opener	ARSENICUM ALBUM, AURUM METALLICUM, CACTUS GRANDIFLORUS, CINCHONA OFFICINALIS, DIGITALIS PURPUREA, KALI CARBONICUM, LITHIUM CARBONICUM, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NAJA TRIPUDIANS, NUX VOMICA, PHOSPHORUS, PULSATILLA (PRATENSIS), PYROGENIUM, SPIGELIA ANTHELMIA	Deseret Biologicals, Inc.	0f398c70-455c-48be-9af3-3eccc96d99a1	2025-05-06	Warnings	Exact identifier ndc (package): 43742-2265-1 ndc (product): 43742-2265 ndc11 (package): 43742226501

Reported adverse events (FAERS/openFDA)#

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