NDC11 43742223801

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
43742-2238-01	43742-2238
43742-2238-1	43742-2238

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
FNG	ADENOSINUM TRIPHOSPHORICUM DINATRUM, ALTERNARIA TENUIS NEES, ASPERGILLUS NIGER, BERBERIS VULGARIS, BRUGIA MALAYI, CANDIDA ALBICANS, CANDIDA PARAPSILOSIS, CARBOLICUM ACIDUM, COCHLEARIA ARMORACIA, ECHINACEA (ANGUSTIFOLIA), FERRUM METALLICUM, FORMALINUM, GLANDULA SUPRARENALIS SUIS, HYDRASTIS CANADENSIS, IRIDIUM METALLICUM, LOMATIUM DISSECTUM, LYCOPODIUM CLAVATUM, METHYLCOBALAMIN, MUCOR RACEMOSUS, MUTABILE BACILLUS (BACH), MYRRHA, PHOSPHORICUM ACIDUM, PROPOLIS, PULSATILLA (PRATENSIS), RHIZOPUS NIGRICANS,	Deseret Biologicals, Inc.	475f5338-7945-4a71-801b-01b1a21f9860	2024-11-20	Warnings	Exact identifier ndc (package): 43742-2238-1 ndc (product): 43742-2238 ndc11 (package): 43742223801

Reported adverse events (FAERS/openFDA)#

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