NDC11 69945005040

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
69945-0050-40	69945-0050
69945-050-40	69945-050

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
OCTREOSCAN	INDIUM IN -111 PENTETREOTIDE	Curium US LLC	93d8f3b2-1216-41dc-a63d-0e812b33891d	2022-02-21	Warnings, Adverse reactions	Exact identifier ndc (package): 69945-050-40 ndc (product): 69945-050 ndc11 (package): 69945005040

Reported adverse events (FAERS/openFDA)#

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