FDA.reportPublic FDA data

NDC11 50090722600

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
50090-7226-050090-7226
50090-7226-0050090-7226

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
FluoxetineFLUOXETINE HYDROCHLORIDEA-S Medication Solutionscdf3b608-e14c-474b-b80e-01ac5f7018662025-10-18Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (package): 50090-7226-0
ndc (product): 50090-7226
ndc11 (package): 50090722600

Reported adverse events (FAERS/openFDA)#

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