NDC11 63323050613

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
63323-0506-13	63323-0506
63323-506-13	63323-506

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Dexamethasone Sodium Phosphate	DEXAMETHASONE SODIUM PHOSPHATE	Fresenius Kabi USA, LLC	cca2c160-9188-48e8-9505-49a52388dcb7	2026-06-30	Warnings, Adverse reactions	Exact identifier ndc (package): 63323-506-13 ndc (product): 63323-506 ndc11 (package): 63323050613
Dexamethasone Sodium Phosphate	DEXAMETHASONE SODIUM PHOSPHATE	Fresenius Kabi USA, LLC	7cbd9005-7df2-47ee-adb3-7244c1c69bc3	2026-06-30	Warnings, Adverse reactions	Exact identifier ndc (product): 63323-506

Reported adverse events (FAERS/openFDA)#

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