NDC11 68083043425

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
68083-0434-2568083-0434
68083-434-2568083-434

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
FurosemideFUROSEMIDEGland Pharma Limited644704c0-e6a5-4804-bfa6-795c8f83aa7a2020-07-03Boxed warning, Warnings, Adverse reactionsExact identifier
ndc (package): 68083-434-25
ndc (product): 68083-434
ndc11 (package): 68083043425

Reported adverse events (FAERS/openFDA)#

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