NDC11 65219044501

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
65219-0445-01	65219-0445
65219-0445-1	65219-0445
65219-445-01	65219-445

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Etomidate	ETOMIDATE	Fresenius Kabi USA, LLC	f38fad46-f2dd-4692-a2a9-a13d0a717bf8	2023-08-10	Warnings, Adverse reactions	Exact identifier ndc (product): 65219-445
Etomidate	ETOMIDATE	Fresenius Kabi USA, LLC	d07efb9e-5264-461d-96d8-e11fa71c5751	2023-07-27	Warnings, Adverse reactions	Exact identifier ndc (package): 65219-445-01 ndc (product): 65219-445 ndc11 (package): 65219044501

Reported adverse events (FAERS/openFDA)#

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