NDC11 00270709973

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
00270-7099-73	00270-7099
0270-7099-73	0270-7099

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
Lumason	SULFUR HEXAFLUORIDE	BRACCO DIAGNOSTICS INC	69822a55-226c-f133-e3b8-2b5826667c5b	2025-12-16	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 0270-7099-73 ndc (product): 0270-7099 ndc11 (package): 00270709973
LumaSon	SULFUR HEXAFLUORIDE	BRACCO DIAGNOSTICS INC	7c679424-c3f7-ed02-892f-20ca0d775089	2025-07-22	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (product): 0270-7099

Reported adverse events (FAERS/openFDA)#

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