FDA.reportPublic FDA data

NDC11 00517182001

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 NDCProduct root
00517-1820-0100517-1820
00517-1820-100517-1820
0517-1820-010517-1820

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 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Chlorothiazide SodiumCHLOROTHIAZIDE SODIUMAmerican Regent, Inc.850960a3-9fe2-4999-81eb-b0ae9ba011bc2020-06-05Warnings, Adverse reactionsExact identifier
ndc (package): 0517-1820-01
ndc (product): 0517-1820
ndc11 (package): 00517182001

Reported adverse events (FAERS/openFDA)#

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