NDC11 65219065050

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
65219-0650-50	65219-0650
65219-650-50	65219-650

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
Midazolam In Sodium Chloride	MIDAZOLAM IN SODIUM CHLORIDE	FRESENIUS KABI USA, LLC	c8f51630-e776-4bc6-ba4d-b714e8c3b8f2	2025-01-31	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 65219-650-50 ndc (product): 65219-650 ndc11 (package): 65219065050

Reported adverse events (FAERS/openFDA)#

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