NDC11 55111053178

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
55111-0531-78	55111-0531
55111-531-78	55111-531

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
divalproex sodium	DIVALPROEX SODIUM	Dr.Reddy's Laboratories Limited	15f8a5be-e269-2e07-60d9-1dd7bf5f5281	2018-12-06	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 55111-531-78 ndc (product): 55111-531 ndc11 (package): 55111053178

Reported adverse events (FAERS/openFDA)#

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