NDC11 70436001506

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
70436-0015-06	70436-0015
70436-0015-6	70436-0015
70436-015-06	70436-015

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 and amlodipine besylate and hydrochlorothiazide	OLMESARTAN MEDOXOMIL AND AMLODIPINE BESYLATE AND HYDROCHLOROTHIAZIDE	Slate Run Pharmaceuticals, LLC	a469adff-25a6-4983-b471-60924d920a86	2025-06-30	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 70436-015-06 ndc (product): 70436-015 ndc11 (package): 70436001506

Reported adverse events (FAERS/openFDA)#

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