NDC11 42291092490

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
42291-0924-90	42291-0924
42291-924-90	42291-924

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
olmesartan medoxomil-hydrochlorothiazide	OLMESARTAN MEDOXOMIL-HYDROCHLOROTHIAZIDE	AvKARE	017bc6a3-5b3d-2381-e063-6394a90abece	2026-01-19	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 42291-924-90 ndc (product): 42291-924 ndc11 (package): 42291092490

Reported adverse events (FAERS/openFDA)#

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