NDC11 00078100768

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
00078-1007-68	00078-1007
0078-1007-68	0078-1007

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
KESIMPTA	OFATUMUMAB	Novartis Pharmaceuticals Corporation	6a8a3f53-2062-48ff-9dbe-b939df133ca3	2026-04-01	Warnings, Adverse reactions	Exact identifier ndc (package): 0078-1007-68 ndc (product): 0078-1007 ndc11 (package): 00078100768

Reported adverse events (FAERS/openFDA)#

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