NDC11 63323058665

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
63323-0586-65	63323-0586
63323-586-65	63323-586

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
Enoxaparin Sodium	ENOXAPARIN SODIUM	Fresenius Kabi USA, LLC	c3be543e-8aff-4311-bf77-e7a5a814ca6f	2026-04-09	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 63323-586-65 ndc (product): 63323-586 ndc11 (package): 63323058665
Enoxaparin Sodium	ENOXAPARIN SODIUM	Fresenius Kabi USA, LLC	a694bbc3-4eb0-4c1e-b4ff-b8abc3e5148e	2025-03-19	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (product): 63323-586

Reported adverse events (FAERS/openFDA)#

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