NDC11 60267031110

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
60267-0311-10	60267-0311
60267-311-10	60267-311

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
NITHIODOTE	SODIUM NITRITE AND SODIUM THIOSULFATE	Hope Pharmaceuticals	ff4941b3-9901-4aab-adcf-c5327bede34e	2025-10-06	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 60267-311-10 ndc11 (package): 60267031110
Sodium Nitrite	SODIUM NITRITE	Hope Pharmaceuticals	52f01c6e-172a-47a9-98a6-9eab7651a032	2025-10-06	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 60267-311-10 ndc (product): 60267-311 ndc11 (package): 60267031110

Reported adverse events (FAERS/openFDA)#

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