NDC11 43742160001

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
43742-1600-01	43742-1600
43742-1600-1	43742-1600

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 Tonsilla Phase	DULCAMARA, ECHINACEA (ANGUSTIFOLIA), AESCULUS HIPPOCASTANUM, ANTIMONIUM TARTARICUM, ASCORBICUM ACIDUM, COCCUS CACTI, GALIUM APARINE, GENTIANA LUTEA, GERANIUM ROBERTIANUM, PULSATILLA (PRATENSIS), SARCOLACTICUM ACIDUM, ACETYLCHOLINE CHLORIDE, MANNOSE, CONIUM MACULATUM, LYMPH NODE (SUIS), SULPHUR, CALCAREA PHOSPHORICA, FUNICULUS UMBILICALIS SUIS, HEPAR SUIS, HYPOTHALAMUS SUIS, MEDULLA OSSIS SUIS, SPLEEN (SUIS), CORTISONE ACETICUM, GLANDULA SUPRARENALIS SUIS, MERCURIUS SOLUBILIS, THYROIDINUM (SUIS),	Deseret Biologicals, Inc.	74f899ed-8021-470a-995b-4822da412c50	2024-05-07	Warnings	Exact identifier ndc (package): 43742-1600-1 ndc (product): 43742-1600 ndc11 (package): 43742160001

Reported adverse events (FAERS/openFDA)#

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