NDC11 65219067201

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
65219-0672-01	65219-0672
65219-0672-1	65219-0672
65219-672-01	65219-672

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
BOMYNTRA	DENOSUMAB	Fresenius Kabi USA, LLC	49d25732-e05d-47e4-98cb-67df04796d4b	2025-03-31	Warnings, Adverse reactions	Exact identifier ndc (package): 65219-672-01 ndc (product): 65219-672 ndc11 (package): 65219067201

Reported adverse events (FAERS/openFDA)#

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