NDC11 73117050901

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
73117-0509-01	73117-0509
73117-0509-1	73117-0509
73117-509-01	73117-509

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
Device - NebuClear MD Hand-held Rubber Bulb Nebulizer	DEVICE - HAND-HELD RUBBER BULB NEBULIZER	Blue Echo Care LLC	43e0a646-be57-1024-e063-6394a90a43e4	2026-05-11	Warnings	Exact identifier ndc (package): 73117-509-01 ndc (product): 73117-509 ndc11 (package): 73117050901

Reported adverse events (FAERS/openFDA)#

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