NDC11 00074104401

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
00074-1044-01	00074-1044
00074-1044-1	00074-1044
0074-1044-01	0074-1044

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
EMRELIS	TELISOTUZUMAB VEDOTIN	AbbVie Inc.	bc04f980-3957-4e35-ab81-8ec2ffe87215	2025-05-25	Warnings, Adverse reactions	Exact identifier ndc (package): 0074-1044-01 ndc (product): 0074-1044 ndc11 (package): 00074104401

Reported adverse events (FAERS/openFDA)#

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