NDC11 51801000815

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
51801-0008-15	51801-0008
51801-008-15	51801-008

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
Dry Eye Test	FLUORESCEIN SODIUM	Nomax Inc.	04866053-f973-471e-b3bc-241fb76303a2	2019-12-23		Exact identifier ndc (package): 51801-008-15 ndc (product): 51801-008 ndc11 (package): 51801000815

Reported adverse events (FAERS/openFDA)#

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