NDC11 33342024307

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
33342-0243-07	33342-0243
33342-0243-7	33342-0243
33342-243-07	33342-243

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 AND HYDROCHLOROTHIAZIDE	Macleods Pharmaceuticals Limited	52c013e1-8c31-4bed-9241-e7845873ebe8	2025-08-04	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 33342-243-07 ndc (product): 33342-243 ndc11 (package): 33342024307

Reported adverse events (FAERS/openFDA)#

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