FDA.reportPublic FDA data

NDC 68982-140 - NUWIQ

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
68982-140
Package NDCs from labels
68982-140-01
Manufacturer
Octapharma USA Inc
Effective date
2024-12-26
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
NUWIQ - Octapharma USA IncOctapharma USA Inc2024-12-26PLASMA DERIVATIVE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68982-140-01NUWIQ2.5 mL in 1 VIALPOWDER, FOR SOLUTION2.5 mL250 [iU] in 2.5mL16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68982-140NUWIQ (ANTIHEMOPHILIC FACTOR (RECOMBINANT)) KIT [OCTAPHARMA USA INC]16Unmatched20250201_d6cb51f8-3acd-412c-93ec-41a8017dff3e.zip

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
WaterACONITUM NAP, ARSENICUM ALB, BORAX, CALC PHOS, GELSENIUM, LYCOPODIUM, PHOSPHORICUM AC, PICRICUM AC, PLUMB MET, SOLIDAGONET Remedies3dc6fdf6-781c-4dec-9aab-a2237fc60c532021-01-19WarningsName fallback
brand name: Water

Reported adverse events (FAERS/openFDA)#

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