NDC11 55150017301

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
55150-0173-01	55150-0173
55150-0173-1	55150-0173
55150-173-01	55150-173

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
Sumatriptan	SUMATRIPTAN	Eugia US LLC	c009976a-4e29-4aeb-9e55-a88766ebb1fb	2025-11-12	Warnings, Adverse reactions	Exact identifier ndc (package): 55150-173-01 ndc (product): 55150-173 ndc11 (package): 55150017301
Sumatriptan	SUMATRIPTAN	Eugia US LLC	9b1bb8c9-be3a-47c3-b3bc-9c983cde7d23	2025-05-29	Warnings, Adverse reactions	Exact identifier ndc (product): 55150-173

Reported adverse events (FAERS/openFDA)#

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