NDC11 43742224001

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
43742-2240-01	43742-2240
43742-2240-1	43742-2240

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, ARTERIA SUIS, ASTRAGALUS EXSCAPUS, BARYTA CARBONICA, CUPRUM SULPHURICUM, DHEA (DEHYDROEPIANDROSTERONE), FUNICULUS UMBILICALIS SUIS, MELILOTUS OFFICINALIS, NATRUM PYRUVICUM, PLACENTA TOTALIS SUIS, PLUMBUM IODATUM, PROTEUS (VULGARIS), QUERCETIN, RUTIN, SARCOLACTICUM ACIDUM, SECALE CORNUTUM, SOLANUM NIGRUM, STROPHANTHUS HISPIDUS, TABACUM, VENA SUIS, VIPERA BERUS	Deseret Biologicals, Inc.	b5ba575a-e8ea-406b-b379-1c4439da01f1	2024-11-18	Warnings	Exact identifier ndc (package): 43742-2240-1 ndc (product): 43742-2240 ndc11 (package): 43742224001

Reported adverse events (FAERS/openFDA)#

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