NDC11 60267070550

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
60267-0705-50	60267-0705
60267-705-50	60267-705

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
Sodium Thiosulfate	SODIUM THIOSULFATE	Hope Pharmaceuticals	82f55408-2de9-463d-85e8-b39c3b259f0b	2026-05-26	Warnings, Adverse reactions	Exact identifier ndc (package): 60267-705-50 ndc (product): 60267-705 ndc11 (package): 60267070550
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): 60267-705-50 ndc11 (package): 60267070550

Reported adverse events (FAERS/openFDA)#

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