NDC11 43742195401

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
43742-1954-01	43742-1954
43742-1954-1	43742-1954

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
Bio Placenta Phase	AESCULUS HIPPOCASTANUM, SARCOLACTICUM ACIDUM, CUPRUM SULPHURICUM, MELILOTUS OFFICINALIS, PLACENTA TOTALIS SUIS, SOLANUM NIGRUM, STROPHANTHUS HISPIDUS, DHEA (DEHYDROEPIANDROSTERONE), QUERCETIN, RUTIN, NATRUM PYRUVICUM, SECALE CORNUTUM, VENA SUIS, ARTERIA SUIS, FUNICULUS UMBILICALIS SUIS, TABACUM, BARYTA CARBONICA, VIPERA BERUS, PLUMBUM IODATUM, ASTRAGALUS EXSCAPUS, PROTEUS (VULGARIS)	Deseret Biologicals, Inc.	e81de491-56b5-46fa-970d-241a38b0f726	2024-09-11	Warnings	Exact identifier ndc (package): 43742-1954-1 ndc (product): 43742-1954 ndc11 (package): 43742195401

Reported adverse events (FAERS/openFDA)#

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