NDC11 51754102901

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
51754-1029-01	51754-1029
51754-1029-1	51754-1029

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
NIPRIDE RTU	SODIUM NITROPRUSSIDE	EXELA PHARMA SCIENCES, LLC	5acf0836-93ff-4064-b888-3f560e8a558d	2018-07-20	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 51754-1029-1 ndc (product): 51754-1029 ndc11 (package): 51754102901

Reported adverse events (FAERS/openFDA)#

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