NDC11 59088080400

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
59088-0804-0	59088-0804
59088-0804-00	59088-0804
59088-804-00	59088-804

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
Lixofen	DICLOFENAC SODIUM, KINESIOLOGY TAPE	PureTek Corporation	1e2a687b-a838-9b16-e063-6394a90a69f3	2025-12-18	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 59088-804-00 ndc (product): 59088-804 ndc11 (package): 59088080400

Reported adverse events (FAERS/openFDA)#

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