NDC11 80425055601

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
80425-0556-01	80425-0556
80425-0556-1	80425-0556
80425-556-01	80425-556

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
DMT SUIK	DEXAMETHASONE SODIUM PHOSPHATE	Advanced Rx of Tennessee, LLC	43045630-8bf8-59ae-e063-6294a90a2ebe	2025-11-07	Warnings, Adverse reactions	Exact identifier ndc (package): 80425-0556-1 ndc (product): 80425-0556 ndc11 (package): 80425055601

Reported adverse events (FAERS/openFDA)#

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