NDC11 00574022901

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
00574-0229-01	00574-0229
00574-0229-1	00574-0229
00574-229-01	00574-229
0574-0229-01	0574-0229

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	Padagis US LLC	3e2d3974-38b0-49d0-8020-f74107584724	2023-05-11	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 0574-0229-01 ndc (product): 0574-0229 ndc11 (package): 00574022901

Reported adverse events (FAERS/openFDA)#

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