NDC11 72536092001

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
72536-0920-01	72536-0920
72536-0920-1	72536-0920
72536-920-01	72536-920

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
Indium In 111 Oxyquinoline	INDIUM IN-111 OXYQUINOLINE	BWXT Medical Ltd.	7dbfc0f9-0e2e-4aed-85bd-32cf7c74d402	2024-11-01	Warnings, Adverse reactions	Exact identifier ndc (package): 72536-0920-1 ndc (product): 72536-0920 ndc11 (package): 72536092001

Reported adverse events (FAERS/openFDA)#

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