FDA.reportPublic FDA data

NDC11 71288020391

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
71288-0203-9171288-0203
71288-203-9171288-203

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 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FurosemideFUROSEMIDEMeitheal Pharmaceuticals Inc.a2e3c748-28ce-4c50-a182-7219129198402026-01-14Warnings, Adverse reactionsExact identifier
ndc (product): 71288-203
FurosemideFUROSEMIDEMeitheal Pharmaceuticals Inc.3aadaca7-3661-4bfe-87f8-6368e4ab65362025-10-06Warnings, Adverse reactionsExact identifier
ndc (package): 71288-203-91
ndc (product): 71288-203
ndc11 (package): 71288020391

Reported adverse events (FAERS/openFDA)#

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