NDC11 43742204701

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
43742-2047-01	43742-2047
43742-2047-1	43742-2047

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
Energize	SARCOLACTICUM ACIDUM, VISCUM ALBUM, IODIUM, FUCUS VESICULOSUS, GALIUM APARINE, THYROIDINUM (SUIS), DHEA (DEHYDROEPIANDROSTERONE), PHENYL ISOTHIOCYANATE, TYRAMINE, ADENOSINUM TRIPHOSPHORICUM DINATRUM, ALPHA-KETOGLUTARICUM ACIDUM, FUMARICUM ACIDUM, MALIC ACIDUM, COLCHICUM AUTUMNALE, CONIUM MACULATUM, NATRUM OXALACETICUM, FUNICULUS UMBILICALIS SUIS, HEPAR SUIS, MEDULLA OSSIS SUIS, PINEAL GLAND (SUIS), SPLEEN (SUIS), THYMUS (SUIS), CALCAREA FLUORICA, PULSATILLA (VULGARIS), SPONGIA TOSTA, CORTISONE ACETICUM	Deseret Biologicals	aaf7ee10-86ae-41db-b0cc-e53d87cb92aa	2024-01-17	Warnings	Exact identifier ndc (package): 43742-2047-1 ndc (product): 43742-2047 ndc11 (package): 43742204701

Reported adverse events (FAERS/openFDA)#

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