NDC11 62559041701

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
62559-0417-01	62559-0417
62559-0417-1	62559-0417
62559-417-01	62559-417

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
Benazepril Hydrochloride and Hydrochlorothiazide	BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE	ANI Pharmaceuticals, Inc.	e6527adf-8c74-4d81-9199-d56a7fca895e	2025-11-26	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 62559-417-01 ndc (product): 62559-417 ndc11 (package): 62559041701

Reported adverse events (FAERS/openFDA)#

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