NDC11 70069050625

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
70069-0506-25	70069-0506
70069-506-25	70069-506

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
Cupric Chloride	CUPRIC CHLORIDE	Somerset Therapeutics, LLC	361d30f2-3c97-4a6c-b252-7fa864d0a625	2026-07-06	Warnings, Adverse reactions	Exact identifier ndc (package): 70069-506-25 ndc (product): 70069-506 ndc11 (package): 70069050625

Reported adverse events (FAERS/openFDA)#

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