NDC11 72819023406

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
72819-0234-06	72819-0234
72819-0234-6	72819-0234
72819-234-06	72819-234

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
CUPRIC CHLORIDE	CUPRIC CHLORIDE	Archis Pharma LLC	45586a5f-4864-4b01-9211-002c77585249	2024-10-16	Warnings, Adverse reactions	Exact identifier ndc (product): 72819-234
CUPRIC CHLORIDE	CUPRIC CHLORIDE	Archis Pharma LLC	77e9dd68-baed-4d62-9284-daecd995de2c	2024-10-14	Warnings, Adverse reactions	Exact identifier ndc (package): 72819-234-06 ndc (product): 72819-234 ndc11 (package): 72819023406

Reported adverse events (FAERS/openFDA)#

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