NDC11 63323049441

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
63323-0494-41	63323-0494
63323-494-41	63323-494

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
Valproate Sodium	VALPROATE SODIUM	Fresenius Kabi USA, LLC	3dfb6da1-f66a-4618-9f74-d2d6c16c0b58	2024-12-15	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 63323-494-41 ndc (product): 63323-494 ndc11 (package): 63323049441
Valproate Sodium	VALPROATE SODIUM	Fresenius Kabi USA, LLC	c572ece7-03d3-4c2a-aeb5-61f2023b28ea	2024-10-24	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (product): 63323-494

Reported adverse events (FAERS/openFDA)#

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