NDC11 55150033701

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
55150-0337-01	55150-0337
55150-0337-1	55150-0337
55150-337-01	55150-337

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
BORTEZOMIB	BORTEZOMIB	Eugia US LLC	ed526447-a4fe-403b-8f08-21ce1b2fa8b7	2025-12-23	Warnings, Adverse reactions	Exact identifier ndc (product): 55150-337
BORTEZOMIB	BORTEZOMIB	Eugia US LLC	76c7c3a5-fd2f-403f-85fd-65a64538eee7	2023-10-20	Warnings, Adverse reactions	Exact identifier ndc (package): 55150-337-01 ndc (product): 55150-337 ndc11 (package): 55150033701

Reported adverse events (FAERS/openFDA)#

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