NDC11 60219158606

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
60219-1586-06	60219-1586
60219-1586-6	60219-1586

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
fluorometholone ophthalmic suspension	FLUOROMETHOLONE	Amneal Pharmaceuticals LLC	e7988a3b-e432-4d42-a8d2-63ca017e6a01	2026-08-12	Warnings, Adverse reactions	Exact identifier ndc (package): 60219-1586-6 ndc (product): 60219-1586 ndc11 (package): 60219158606

Reported adverse events (FAERS/openFDA)#

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