NDC11 43742157901

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
43742-1579-01	43742-1579
43742-1579-1	43742-1579

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
Metab	ASCORBICUM ACIDUM, CYSTEINUM, MANGANESE GLUCONATE, ALPHA-KETOGLUTARICUM ACIDUM, FUMARICUM ACIDUM, GERMANIUM SESQUIOXIDE, IODIUM, MAGNESIUM METALLICUM, NATRUM OXALACETICUM, PULSATILLA (PRATENSIS), THYROIDINUM (SUIS), VANADIUM METALLICUM	Deseret Biologicals, Inc	fbf89a37-dca2-4498-8866-234b033c5d42	2023-01-12	Warnings	Exact identifier ndc (package): 43742-1579-1 ndc (product): 43742-1579 ndc11 (package): 43742157901

Reported adverse events (FAERS/openFDA)#

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