NDC11 43742137901

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
43742-1379-01	43742-1379
43742-1379-1	43742-1379

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
Male Stimulant	ARALIA QUINQUEFOLIA, AGNUS CASTUS, ASCORBICUM ACIDUM, CALADIUM SEGUINUM, KALI BROMATUM, CANTHARIS, DAMIANA, FUNICULUS UMBILICALIS SUIS, GLANDULA SUPRARENALIS SUIS, HYPOPHYSIS SUIS, ORCHITINUM (SUIS), PROSTATE (SUIS), STRYCHNINUM PHOSPHORICUM, CONIUM MACULATUM, DIENCEPHALON (SUIS), HEART (SUIS), FERRUM PHOSPHORICUM, MAGNESIA PHOSPHORICA, SELENIUM METALLICUM, ZINCUM METALLICUM, PINEAL GLAND (SUIS), CORTISONE ACETICUM, MANGANUM PHOSPHORICUM, LYCOPODIUM CLAVATUM, TESTOSTERONE, MORGAN GAERTNER	Deseret Biologicals, Inc.	d48437d6-a54f-4e11-bcfb-9e0d5c1e98da	2024-04-15	Warnings	Exact identifier ndc (package): 43742-1379-1 ndc (product): 43742-1379 ndc11 (package): 43742137901

Reported adverse events (FAERS/openFDA)#

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