NDC11 70436020680

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
70436-0206-80	70436-0206
70436-206-80	70436-206

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
sodium nitroprusside in 0.9% sodium chloride	SODIUM NITROPRUSSIDE IN 0.9% SODIUM CHLORIDE	Slate Run Pharmaceuticals, LLC	6f02e4ac-5f7c-4003-b9b7-283f489cddb0	2023-11-15	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 70436-206-80 ndc (product): 70436-206 ndc11 (package): 70436020680

Reported adverse events (FAERS/openFDA)#

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