NDC11 42571024505

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
42571-0245-05	42571-0245
42571-0245-5	42571-0245
42571-245-05	42571-245

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, AMLODIPINE and HYDROCHLOROTHIAZIDE	OLMESARTAN MEDOXOMIL, AMLODIPINE BESYLATE AND HYDROCHLOROTHIAZIDE	Micro Labs Limited	9fb71df8-f70f-47dc-9465-8d8748261caf	2025-11-29	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 42571-245-05 ndc (product): 42571-245 ndc11 (package): 42571024505

Reported adverse events (FAERS/openFDA)#

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