NDC11 80725060018

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
80725-0600-18	80725-0600
80725-600-18	80725-600

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
Eulexin	FLUTAMIDE	Waylis Therapeutics LLC	56b6ba36-9b49-4422-a2a4-7bfa0d941a5d	2022-01-13	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 80725-600-18 ndc (product): 80725-600 ndc11 (package): 80725060018

Reported adverse events (FAERS/openFDA)#

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