NDC11 55150032001

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
55150-0320-01	55150-0320
55150-0320-1	55150-0320
55150-320-01	55150-320

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	SODIUM NITROPRUSSIDE	AuroMedics Pharma LLC	41e11afb-5fa4-4212-889d-1092dbd0702a	2020-12-12	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 55150-320-01 ndc (product): 55150-320 ndc11 (package): 55150032001

Reported adverse events (FAERS/openFDA)#

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