NDC11 43857063101

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
43857-0631-01	43857-0631
43857-0631-1	43857-0631
43857-631-01	43857-631

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
Diathesis IV	GINKGO BILOBA, FEL TAURI, KIDNEY (SUIS), GERMANIUM SESQUIOXIDE, ARGENTUM METALLICUM, CUPRUM METALLICUM, CYSTEINUM, AURUM METALLICUM, MANGANESE GLUCONATE, ALPHA-KETOGLUTARICUM ACIDUM, FUMARICUM ACIDUM, MERCURIUS SOLUBILIS, NATRUM OXALACETICUM, NUX VOMICA, PHOSPHORICUM ACIDUM	BioActive Nutritional, Inc.	74b5157f-c33f-494a-ab61-0e0a547b5f4a	2023-04-13	Warnings	Exact identifier ndc (package): 43857-0631-1 ndc (product): 43857-0631 ndc11 (package): 43857063101

Reported adverse events (FAERS/openFDA)#

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